IQVIA

IQVIA est le leader mondial dans l’apport  de données de santé et de données pharmaceutiques au secteur des soins de santé. Notre division Real World Solutions (RWS) est reconnue à l’échelle mondiale pour offrir des recherches axées sur les enjeux d’affaires, réalisées selon les normes les plus élevées. IQVIA propose une gamme de services permettant aux acteurs du secteur de la santé d’accéder aux données issues du monde réel et de les exploiter pour prendre des décisions à chaque étape du cycle de vie des produits. L’équipe canadienne de RWS se concentre sur la prestation de solutions innovantes pour les équipes d’accès au marché, HEOR, médicales et scientifiques. L’équipe RWS Canada est un groupe diversifié et multidisciplinaire engagé envers l’excellence et le travail d’équipe. Responsabilités fonctionnelles Soutenir la supervision et la livraison d’un large éventail de projets clients en oncologie dans les domaines pharmaceutique et des dispositifs médicaux au Canada, notamment des projets d’accès au marché, des études rétrospectives basées sur des bases de données, des stratégies commerciales, des analyses économiques de la santé, des parcours patients, des mesures d’accès ainsi que d’autres mandats variés et stimulants. Ce rôle mettra l’accent sur le développement de solutions en accès au marché, stratégie commerciale et évaluations des technologies de la santé (ETS) pour des clients en oncologie. En collaboration avec les autres membres de l’équipe, vous devrez : Gérer des projets et contribuer à la conception des études et au développement des méthodologies Élaborer des approches, cadres et solutions innovants pour répondre aux problématiques clients Réviser et contribuer à la préparation de propositions, protocoles d’études et rapports préliminaires Interpréter des données qualitatives et quantitatives issues du monde réel pour les livrables Superviser et préparer des stratégies d’accès au marché destinées aux soumissions auprès des parties prenantes, incluant les agences d’Évaluation des technologies de la santé , L'Agence des médicaments du Canada  (AMC)/INESSS, l’Alliance pancanadienne pharmaceutique (APP) et les payeurs Préparer des présentations, résumés scientifiques et manuscrits pour des congrès et publications Réaliser et superviser des recherches de marché primaires et secondaires Diriger et animer des ateliers, comités consultatifs d’experts et des discussions modérées Réaliser et superviser des recherches qualitatives et quantitatives auprès des leaders d’opinion au Canada Contribuer à l’élaboration et à la présentation de contenus de réflexion stratégique , livres blancs, affiches scientifiques et matériel de conférence Les associés principaux sont responsables de la gestion simultanée de plusieurs projets de consultation de complexité variable, en assurant le respect des échéanciers et des budgets pour les clients des sciences de la vie. Ils contribuent également au développement des affaires, au maintien et au renforcement des relations clients, et peuvent appuyer le développement de nouvelles offres. Gestion de projet et relations avec les clients Soutenir la gestion globale des projets et de la relation client Participer à des réunions avec les clients et partenaires externes, généralement avec un collègue Agir, avec les consultants séniors, comme point de contact clé auprès des clients, en apportant des solutions innovantes et une expertise en accès au marché Des déplacements chez les clients peuvent être requis Développement des affaires Analyser les besoins des clients pour élaborer des propositions dépassant leurs attentes Rédiger et affiner des propositions en réponse aux appels d’offres en collaboration avec les clients Travailler étroitement avec les collègues Directeurs et Directeurs principaux pour développer de nouvelles opportunités Contribuer à la croissance stratégique de l’offre en oncologie, notamment en accès au marché, en tirant parti des stratégies fondées sur les données du monde réel  et des plans de mise en marché Expérience 5 à 10 ans d’expérience dans l’industrie pharmaceutique ou en consultation, en accès au marché ou en économie de la santé Expérience confirmée dans la direction de mandats de consultation Expérience dans un ou plusieurs des secteurs suivants : consultation en santé, industrie pharmaceutique/soins de santé, milieux universitaires ou organismes de recherche gouvernementaux, ou recherche en services de santé Compétences techniques et connaissances (atouts) Bonne connaissance des processus de remboursement pharmaceutique au Canada Expérience en analyse de bases de données et/ou de registres Analyse de données longitudinales au niveau des patients Bonne compréhension des théories en recherche sur les résultats en santé et connaissance pratique de la mise en œuvre de projets de recherche Solides compétences quantitatives et analytiques Maîtrise de Word, PowerPoint et Excel Capacité à rédiger des rapports et manuscrits clairs, précis et concis Compréhension du système de santé canadien et international Expérience avec VBA dans Excel (atout) Expérience avec des logiciels statistiques (SAS, SPSS, R) (atout) Sens des affaires et compréhension du secteur des technologies de la santé et de l’industrie pharmaceutique Connaissance des méthodes, outils et techniques en consultation Compétences personnelles et comportements Pensée logique et capacité à résoudre des problèmes de façon créative Fort engagement envers la qualité du travail et l’amélioration continue Excellentes aptitudes en communication Capacité d’adaptation à différents contextes et styles de travail Esprit d’équipe avec sens des responsabilités et proactivité Solides capacités d’analyse, d’interprétation et de résolution de problèmes Capacité à prioriser efficacement et à gérer son temps dans un environnement dynamique Potentiel démontré en leadership et intérêt pour une progression de carrière à long terme Motivation à apprendre et à relever de nouveaux défis Formation Doctorat (PhD) / maîtrise / MBA dans un domaine pertinent des sciences de la santé ou expérience équivalente Formation clinique (MD, PharmD, IPS, etc.) considérée comme un atout Bilinguisme français et anglais fortement préférable IQVIA is the world leader in the provision of health and pharmaceutical data to the health care sector. Our Real World Solutions department is globally renowned for providing business-focused research conducted to the highest standards. IQVIA delivers a suite of services to help healthcare stakeholders access and apply real-world evidence for decisions at every stage of the product lifecycle. The Canadian Real World Solutions team is focused on providing innovative solutions for Market Access, HEOR, medical, and scientific teams. The RWS Canada team is a diverse, multidisciplinary group dedicated to excellence through teamwork. Functional Responsibilities Support the oversight and delivery of a wide range of oncology client projects in the pharmaceutical and medical device space in Canada, including market access projects, retrospective database studies, business strategy, health economic analyses, patient journeys, access metrics, and other varied and exciting engagements. This role will focus on driving solutions in Market Access, Business Strategy, and HTA for oncology clients. Working with other team members, you will: Project manage and contribute to study design and methodology development Develop innovative approaches, frameworks, and solutions to client problems Review and assist in the preparation of proposals, study protocols, and draft reports Interpret qualitative and quantitative real-world data for deliverables Oversee and prepare market access strategies that will be leveraged for submissions to stakeholders including HTA, PCPA, and payers Prepare presentations, abstracts, and manuscripts for scientific conferences and journals Conduct and oversee primary and secondary market research Lead and facilitate workshops, expert advisory boards, and moderated discussions Conduct and oversee qualitative and quantitative research with Canadian opinion leaders Support the development and presentation of thought leadership pieces, white papers, posters, and conference materials Associate Principals are responsible for overseeing and managing multiple consulting projects of varying complexity and ensuring on-time, on-budget delivery for life sciences clients. They contribute to new business development, maintain and strengthen the client base, and may support the development of new offerings. Project Management and Client Liaison Responsibilities Assist with overall project and client management Attend client and external meetings, typically alongside a colleague Along with senior consultants, serve as an additional key point of contact for clients, driving innovative solutions and providing Market Access expertise Travel to client sites may be required Business Development Responsibilities Review and analyze client requirements to develop proposals that exceed expectations Produce and refine proposals in response to client RFPs in collaboration with clients Work closely with Principals and Senior Principals on opportunities to grow the business Support the drive for strategic growth in the Oncology solution space with a focus on market access, leveraging real-world evidence (RWE) strategies and go to market planning. Experience 5–10 years’ experience in the pharmaceutical or consulting industry in Market Access or Health Economics Proven experience leading consulting engagements Experience gained in one or more of the following: Healthcare consulting, pharmaceutical/healthcare industry, academic or government research organizations, or health services research settings Technical Skills and Knowledge (Assets) Good understanding of the pharmaceutical reimbursement process in Canada Conducting analyses in databases and/or registries Longitudinal patient-level data analysis Good understanding of outcomes research theory, and practical knowledge of research project implementation Strong quantitative and analytical skills Proficiency with Word, PowerPoint, and Excel Ability to write reports and manuscripts in clear, accurate, and concise language Understanding of and interest in the Canadian and international healthcare environment Experience with VBA in Excel is a plus Experience with statistical software (SAS, SPSS, R) is a plus Commercial awareness and understanding of the health technology and pharmaceutical industry Knowledge of consulting methods, tools, and techniques Personal Skills and Behaviors Logical thinker and creative problem solver Strong commitment to high-quality work and continuous improvement Excellent communication skills Ability to adapt to different situations and working styles Team player with a proactive, ownership-oriented mindset Strong analytical, interpretive, and problem-solving capabilities Ability to prioritize effectively and manage time in a fast-paced environment Demonstrated leadership potential and interest in long-term career growth Eagerness to learn and take on new challenges Education Requirements PhD / Master’s / MBA in a relevant health sciences field or equivalent experience Clinical qualifications a plus (MD, PharmD, NP, etc.) Bilingual in French & English highly preferred IQVIA est un fournisseur mondial de premier plan de services de recherche clinique, d'informations commerciales et de renseignements sur les soins de santé pour les secteurs des sciences de la vie et de la santé.  IQVIA se consacre à accélérer le développement et la commercialisation de traitements médicaux innovants pour aider à améliorer les résultats des patients et la santé de la population dans le monde entier. Pour en savoir plus, visitez https://jobs.iqvia.com   IQVIA est fière d’être un employeur souscrivant au principe de l’égalité d’accès à l’emploi. Tous les candidats qualifiés seront pris en considération pour un emploi sans égard à la race, la couleur, la religion, le sexe, l’orientation sexuelle, l’identité de genre, l’origine nationale, le handicap, l’âge, l’état matrimonial ou tout autre statut protégé par la loi applicable.  Des mesures d’adaptation pour les candidats handicapés sont disponibles sur demande dans tous les aspects du processus de recrutement. Si vous avez un handicap qui nécessite une mesure d’adaptation, nous vous encourageons à contacter notre équipe d’acquisition de talents au [email protected], afin qu’IQVIA puisse soutenir votre participation au processus de recrutement. IQVIA s’engage à faire preuve d’intégrité dans son processus de recrutement et applique une politique de tolérance zéro en matière de fraude des candidats. Toutes les informations et toutes les qualifications soumises dans votre candidature doivent être véridiques et complètes. Toute fausse déclaration, présentation trompeuse ou omission importante au cours du processus de recrutement entraînera la disqualification immédiate de votre candidature, ou la cessation d’emploi si elle est découverte ultérieurement, conformément aux lois applicables. Nous apprécions votre honnêteté et votre professionnalisme. Veuillez noter qu'il est possible que nous utilisions l'intelligence artificielle (IA) dans le traitement de votre candidature. Cependant, nous utilisons l'IA uniquement pour aider notre équipe de recrutement à sélectionner ou à évaluer les candidatures, et non pas pour remplacer la prise des décisions par les membres de notre équipe. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, marital status, or any other status protected by applicable law.  Accommodations for applicants with disabilities are available in all aspects of the recruitment process upon request. If you have a disability that requires an accommodation, we encourage you to contact our Talent Acquisition Team at: [email protected], so that IQVIA can support your participation in the recruitment process. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. Please note that we may use artificial intelligence (AI) in the processing of your application. However, we only use AI to assist our recruitment team with the screening or assessment of candidacies, and not as a substitute for human decision-making. La fourchette salariale de base potentielle pour ce poste, annualisée, est de $118,800.00 - $168,800.00. Le salaire de base réel offert peut varier selon plusieurs facteurs, notamment les qualifications liées à l’emploi telles que les connaissances, les compétences, la formation et l’expérience; l’emplacement; et/ou l’horaire (temps plein ou temps partiel). Selon le poste offert, des régimes d’incitation, des primes et/ou d’autres formes de rémunération peuvent être proposés, en plus d’une gamme d’avantages sociaux liés à la santé, au bien-être et/ou d’autres bénéfices.  The potential base pay range for this role, when annualized, is $118,800.00 - $168,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and wellness and/or other benefits.

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, Technology, analytics and human ingenuity to drive healthcare forward. Global Product Specialist / Consultant - Digital Commercial Solutions Job Overview OneKey Marketing Services is entering into a new dimension to provide communication services to Life Science companies that request to enlarge their communication capacity by using more personal communication channels. Therefore, we must build the global programmatic offering, with a mix of acquisition, partnership and skills development. Responsibilities As a Product Specialist, you will oversee: Product promotion through a strategic roadmap 3 years including market research. Evangelization of programmatic advertising Competitive Intelligence: Landscape, competitors, new technology Sales Monitoring: ROI, Forecast Lead and coordinate all activities related to the promotion and raising awareness of the service. Research and identify new business opportunities - including new markets, growth areas, trends, customers, partnerships, products, and services - or new ways of reaching existing markets. Seek out the appropriate contact in an organisation. Generate leads and cold call prospective customers. Meet with customers/clients face to face or over the phone. Foster and develop relationships with customers/clients. Understand the needs of your customers and be able to respond effectively with a plan of how to meet these. Think strategically - seeing the bigger picture and setting aims and objectives to develop and improve the business. Work strategically - carrying out necessary planning to implement operational changes. Have a good understanding of the businesses' products or services and be able to advise others about them. Ensure staff are on board throughout the organisation and understand the need for change and what is required of them. Train members of local sales team, arranging external training where appropriate Discuss promotional strategy and activities with the marketing department. Liaise with the finance team, warehousing, and logistics departments as appropriate. seek ways of improving the way the business operates. Attend seminars, conferences, and events where appropriate. Keep abreast of trends and changes in the business world. Track revenue and work collaboratively with the programmatic product lead. Qualifications & Skills - Our Ideal Candidate Will Have Around 5 years of experience in managing and developing accounts across agencies, trading desks or brands directly. Strong understanding of the programmatic landscape Experience working in digital media, with hands-on experience and deep understanding of programmatic and media sales (DSP, SSP, publisher, Ad Network) Tenacity and drive to seek new business and meet or exceed targets. Interpersonal skills for building and developing relationships with clients. Written and verbal communication skills in English Teamworking skills and a collaborative approach to work Ability to multitask and prioritise. Project management and organisational skills Negotiation skills Ability to think strategically. Ability to analyse sales figures and write reports. A flexible approach to work with the ability to adapt to a fast-paced, ever-changing environment. Please submit your cv in English! We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™. IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

As the only global provider of commercial solutions, IQVIA understands what it takes to deliver nationally and internationally. Our teams help biopharma get their medicines to the people who need them. We help customers gain insight and access to their markets and ultimately demonstrate their product's value to payers, physicians and patients. A significant part of our business is acting as the biopharma's field force to physicians or providing nurses to educate patients or prescribers. With the right experience, you can help deliver medical breakthroughs in the real world. We are excited to announce that we are looking for a Clinical Specialist to join our team of over 10,000 global field representatives in several regions making over 20 million product details annually for our pharmaceutical and biotech clients.   Operating Room Clinical Nurse The Biosurgery Clinical Specialist provides clinical assessments on adjunctive hemostat device needs, risks, recommendations and implementation recommendations to customers (primarily nurses, educators, risk managers, surgeons and techs).  This role plays an integral part in gathering key insights on utilization, techniques, applications based by specialty or service lines, capturing documenting and sharing these insights with the US Marketing team and partnering with local sales team to work collaboratively with sales management and the sales representative to gain appropriate access into aligned pilot accounts. Pivotal to the success of the candidate will be his/her ability to develop effective working relationships with the customers in the assigned territory. The incumbent must be able to work autonomously, be knowledgeable in adjunctive hemostats and confidently interact with clinical personnel and management.  The candidate chosen for this role will be expected to: Complete training on adjunctive hemostat devices and products to be proficient in product utilization and demonstration.Demonstrate mastery of all clinical information related to product application and the IFU; must be able to use this mastery to help drive and convert business by upgrading to more advanced brands. Develop strong, working relationships with surgical leadership and clinicians while providing adjunctive hemostat recommendations and bleeding risk assessments.  Educate OR nurses, techs and physicians on the proper techniques to effectively capture real-world utilization data by specialty/service lines.Conduct pilot account assessments, develop Analysis and present recommendations to management.Educate and inform end-users of clinical effectiveness of adjunctive hemostat products and technical aspects of Ethicon’s products.Present adjunctive hemostat recommendations and assist with implementation.Participate in adjunctive hemostat product evaluations as necessary within the aligned Pilot accounts.Assist field sales in collection of product utilization and performance data to support team business case.Present adjunctive hemostat continuing education programs to clinical and leadership groups within aligned accounts.Communicate educational content and distribute materials and programs. Assist US Marketing in identifying Key Opinion Leaders, upgrade opportunities and provide presentations of clinical data outcomes to end-users. Participate in key society meetings as appropriate.Requirements Qualifications/Experience 4 year Bachelor's degree required (degree in nursing, business or related field is preferred.)Valid RN license in state of residency requiredA minimum of 5 years clinical experience requiredA minimum of 3 years OR experience requiredStrong group presentation skills and experience in presenting clinical education and/or surgical leadership/management.   Specialty CNOR certification or related specialty is preferred.Excellent written and verbal communication skillsAssertive, ability to work independently and uncover opportunitiesAbility to plan and deliver formal presentations (large and small groups)Excellent written and verbal communication and organizational planning skills, including time and territory management and structured thinking in clinical procedure settings.Familiarity with AORN Surgical Smoke Safety GuidelinesStrong MS Office, Word, Excel skillsCompetencies The Biosurgery Clinical Specialist promotes the Ethicon culture through positive, ongoing customer relationships.This position also requires the ability to develop strong relationships with customers and within the Ethicon teamMust have the ability to work both as a partner with sales, marketing and commercial teammates and autonomously in the field, as needed.The ability to display decisiveness and an understanding of business acumen in clinical situations is required.Must have the ability to work collaboratively with other Ethicon team members to ensure open communication of ideas and techniques.   Must be highly organized and self-directed. Employee performance will be compared with other clinical specialists’ feedback provided accordingly.   Candidates must have a valid driver's license.As a salaried position, the hours are not restricted to “normal business hours” and ability to work flexible hours during days, nights and/or weekends as necessary is required.Travel is required as part of the position (approx. 75%).This position is bonus eligible, and the employee’s ability to meet the above requirements has a direct impact on this compensation.IQVIA offers a friendly, progressive work atmosphere and a comprehensive benefits package including medical, dental, life insurance and vision coverage, tuition assistance, bonus plan and 401(k). IQVIA is an EEO Employer - Minorities/Females/Protected Veterans/Disabled We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™. We look forward to the prospect of working with you! Please apply on-line at: www.IQVIA.com #LI-CES IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is $100-135,000 annually. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen. Werden Sie Teil unserer Community von rund 86.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welche Rolle Sie bei IQVIA einsteigen, es erwartet Sie ein offenes, innovationsfreudiges Umfeld, in dem Sie sich viel bewegen können. Finden Sie heraus, wie Sie Ihre Talente und Ihre Leidenschaften bei IQVIA einbringen können. Im Bereich Commercial Engagement Services (CES) arbeiten wir eng mit unseren Life Sciences-Kunden zusammen und unterstützen sie mit flexiblen Vertriebs- und Personallösungen für nachhaltigen Erfolg am Markt. Dies umfasst insbesondere die Rekrutierung, das Training und die Steuerung des Vertriebsteams in Dienstleistungsprojekten bzw. in Arbeitnehmerüberlassung. Dabei differenzieren wir uns über integrierte Projektansätze entlang des IQVIA Lösungsportfolios, die wir individuell an die Kundenbedürfnisse anpassen und aus einer Hand anbieten. Komm in unser Team! Für einen bundesweiten Teamaufbau suchen wir Regionalleiter (m/w/d) zum nächstmöglichen Zeitpunkt mit Engagement und Begeisterungsfähigkeit. im Gebiet: Süd-Ost Das sind Deine Aufgaben: Als Regionalleiter bist Du ein wichtiges Bindeglied zwischen der Unternehmensführung, dem nationalen Vertriebsleiter sowie dem Vertriebsteam und der Zielgruppe.In dieser Rolle verantwortest Du die Vertriebsergebnisse Deiner Region und führst ein schlagkräftiges Außendienstteam aus Pharmaberatern zur Absatzsteigerung von Impfstoffen bei Allgemeinmedizinern, Praktiker und Internisten.Führung, Coaching und Motivation Deines Teams haben für Dich oberste Priorität, um erfolgreiche Verkaufsgespräche beim Arzt sicherzustellen und Deine Mitarbeiter für die gemeinsamen Ziele zu begeistern.Verantwortung für eine effektive Planung, Koordination und Steuerung aller Außendienstaktivitäten Deines TeamsZur Sicherstellung der Zielerreichung pflegst Du eine enge Abstimmung und Zusammenarbeit mit der Vertriebsleitung.Analyse der KPIs zur Ableitung von Maßnahmenplänen zur kontinuierlichen Entwicklung der VertriebsgebieteDas wünschen wir uns von Dir: Du hast bereits mehrere Jahre erfolgreich als Regionalleiter im Pharma-Außendienst gearbeitet, idealerweise im Bereich Impfstoffe, und suchst jetzt nach einer neuen Herausforderung.Wie Deine Mitarbeiter im Team hast auch Du die notwendige Qualifikation gemäß §75 AMG, um die gesetzlichen Vorgaben im Arzt-Außendienst zu erfüllen.Als erfahrener Regionalleiter beherrschst Du nicht nur moderne Führungsinstrumente, sondern verstehst es auch, Deine Mitarbeiter für gemeinsame Ziele zu begeistern und ihr Potenzial zu fördern.Du bist leistungsorientiert und durchsetzungsstark und verstehst es, Dein Team immer wieder zu Höchstleistungen zu motivieren.Deine ausgeprägte Zahlenaffinität und starke analytische Fähigkeiten konntest Du bereits in vorherigen Aufgaben unter Beweis stellen und entwickelst diese konsequent weiter.Die richtige Mischung aus Motivation und Kompetenz ist die Basis für Deinen Erfolg und dafür setzt Du dich als Regionalleiter jeden Tag ein.Darauf darfst du Dich freuen: In unserer Arbeitskultur legen wir großen Wert auf Zusammenarbeit, Respekt und gegenseitige Unterstützung. Wir fördern eine Umgebung, in der sich jeder willkommen und wertgeschätzt fühlt. Offene Kommunikation und Transparenz sind für uns essenziell, um Vertrauen und ein starkes Gemeinschaftsgefühl zu schaffen.Ein attraktives Gehaltspaket plus Kundenprämien, vielfältige Corporate Benefits, betriebliche Altersvorsorge sowie 24/7 Unfallversicherung (auch für den privaten Bereich) und exklusive private KrankenzusatzversicherungenEin top ausgestatteter Firmenwagen verschiedener Premiumanbieter mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des Modells  Eine moderne IT-Ausstattung für Deinen modernen digitalen ArbeitsplatzUnser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige PerspektiveWir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines WohnortsEine hohe Übernahmequote durch unsere Kunden ermöglicht Dir den Karrierestart bei zukunftsweisenden und führenden Unternehmen der Pharmabranche und Medizintechnik-BrancheVielfältige und individuelle Weiterentwicklungsmöglichkeiten auch innerhalb von IQVIA (z.B. Führung, Key Account Management, Projektmanagement und vieles mehr)Wir begleiten Dich während Deiner Bewerbungsphase durch individuelle Betreuung/Vorbereitung bis zur Einstellung und auch darüber hinaus während des BeschäftigungsverhältnissesUnser Kunden-Netzwerk reicht vom Start-up Unternehmen bis zum Global Player. Gemeinsam mit Dir finden wir den richtigen Job für Dich! Starte Deine Karriere mit IQVIA! Dein besonders schneller Draht zu uns: Kandidaten-Hotline: 0621-84508113 oder sende uns gerne direkt Deine Bewerbung per Mail an: [email protected] , besser noch lade deinen Lebenslauf direkt nach deiner Registrierung in Workday hoch. Hier der Link: Workday #LI-CES #LI-DNP #LI-SS2 #Pharmaberater #Biologie #Chemie #Pharmareferent #BTA #CTA #PTA #MTA #Oecotrophologie #Pharmazie #Pharma-Außendienst IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA Overview:IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. Our work accelerates the development and commercialization of medical treatments that improve patient outcomes and population health worldwide. With a multidisciplinary team of 88000+ experts spanning data science commercialization regulatory and technology IQVIA empowers its consultants to translate the world’s most pressing healthcare challenges into actionable strategies that speed new therapies to market.Job Overview:The Project Manager will spearhead the end-to-end implementation and delivery of projects across various stakeholders ensuring alignment with contractual commitments and client objectives. This role involves defining establishing and managing implementation delivery expectations across programs using a hybrid project management approach ensuring successful execution and client satisfaction.Responsibilities:Lead the complete project lifecycle including initiation planning execution monitoring and closure ensuring delivery within contractual timelines and scope.Develop and maintain detailed project plans and timelines using Smartsheet covering dependencies milestones risks and resource allocation.Manage delivery within compressed timelines proactively identifying risks and implementing mitigation strategies to ensure schedule adherence.Establish and enforce change management and change control processes including documentation and stakeholder alignment to manage and mitigate scope creep.Coordinate and lead cross-functional teams to ensure seamless execution of deliverables.Manage and coordinate with third-party vendors and external partners ensuring alignment with project objectives timelines and quality standards.Lead client-facing governance including status reporting risk/issue escalation and executive-level communication.Conduct and lead client and internal status meetings ensuring clear documentation of actions risks and decisions.Maintain all project documentation RAID logs and deliverables in compliance with organizational standards.Qualifications:Bachelor’s Degree preferred; PMP (Project Management Professional) certification preferred.Proven experience managing complex projects in fast-paced client-facing environments.Demonstrated expertise in project management tools with Smartsheet preferred for planning tracking and reporting.Experience managing scope risks dependencies and issue resolution across large-scale programs.Proven ability to deliver within compressed timelines and high-pressure environments.Experience managing cross-functional teams and third-party vendors.Strong stakeholder management and communication skills including executive-level reporting.Ability to manage multiple projects and priorities simultaneously.Highly organized with the ability to maintain detailed documentation and governance artifacts.Demonstrated ownership accountability and ability to drive outcomes independently.Experience leveraging Microsoft Copilot to enhance project delivery and documentation.Experience in pharmaceutical patient support services (PSS) copay or HUB programs preferred.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $78,700.00 - $196,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Aperçu du posteFournit des contributions de haute qualité et ponctuelles aux projets clients dans le domaine des sciences de la vie. Les missions nécessitent généralement une analyse et une résolution de problèmes dans un cadre établi. Fonctions essentielles Sous supervision directe, aide à l'examen et à l'analyse des besoins ou des problèmes des clients, et contribue au développement de solutions adaptées. Participe à l'élaboration de la documentation détaillée et des spécifications. Sous supervision étroite, réalise des analyses quantitatives ou qualitatives afin d'identifier les problématiques clients et d’élaborer des solutions spécifiques. Contribue à la conception et à la structuration de présentations adaptées aux caractéristiques et aux besoins du public cible. Développe proactivement une connaissance de base des méthodologies de conseil et du marché des sciences de la vie à travers la réalisation de missions de conseil et la participation à des opportunités d’apprentissage formelles et informelles. Les responsabilités liées aux missions sont attribuées et étroitement encadrées par des Consultants, Consultants Seniors, Chefs de mission ou Associés. Qualifications En cours d’obtention d’une licence1 à 3 ans d’expérience pertinente requis Collabore volontiers et efficacement avec les autres au sein de l’organisation pour atteindre les objectifs de l’équipe. Connaissance et compréhension des processus fondamentaux de l’entreprise, de leurs interactions, et de l’impact des influences internes/externes sur les prises de décisions, la croissance et le déclin. Maîtrise des méthodes, outils et techniques de conseil liés à son domaine fonctionnel. Connaissance des événements actuels et des évolutions dans une industrie donnée ainsi que des principaux concurrents. Compréhension du marché. Connaissance des associations professionnelles/commerciales, des personnes clés et des entreprises. Capacité efficace de gestion du temps. Vous devrez travailler directement avec des départements, des équipes, des fonctions de support et des parties prenantes d'IQVIA situés partout au Canada et à travers le monde, par conséquent, une connaissance fonctionnelle de l'anglais, tant à l'écrit qu'à l'oral, est nécessaire à l'exercice des fonctions de ce poste. ---------------------------------------------- Job Overview Provides high quality, on-time input to client projects in the life sciences field. Assignments typically require analysis and problem solving within an established framework. Essential Functions• Under direct supervision, assists with the review and analysis of client requirements or problems and assists in the development of client solutions.• Assists in the development of detailed documentation and specifications.• Under close supervision, performs quantitative or qualitative analyzes to assist in the identification of client issues and the development of client specific solutions.• Assists in the design and structure of presentations that are appropriate to the characteristics or needs of the audience.• Proactively develops a basic knowledge of consulting methodologies and the life sciences market through the delivery of consulting engagements and participation in formal and informal learning opportunities.• Engagement based responsibilities are assigned and closely managed by Consultants, Senior Consultants, Engagement Managers or Principals. Qualifications • Pursuing Bachelor's Degree • 1-3 years of related experience • Works willingly and effectively with others in and across the organization to accomplish team goals. • Knowledge and understanding of the fundamental processes of business, their interaction, and the impact of external/internal influences on decision making, growth and decline. • Knowledge of consulting methods, tools and techniques, related to one’s functional area. • Knowledge of current events and developments within an industry and major competitors. • Knowledge and understanding of the marketplace. Knowledge of professional/trade associations, key people and companies. • Effective time management skills. You will be required to work directly with IQVIA departments, teams, support functions and stakeholders located across Canada and around the world therefore, a functional knowledge of English, both written and spoken, is necessary to perform the duties of this position. IQVIA est un fournisseur mondial de premier plan de services de recherche clinique, d'informations commerciales et de renseignements sur les soins de santé pour les secteurs des sciences de la vie et de la santé.  IQVIA se consacre à accélérer le développement et la commercialisation de traitements médicaux innovants pour aider à améliorer les résultats des patients et la santé de la population dans le monde entier. Pour en savoir plus, visitez https://jobs.iqvia.com   IQVIA est fière d’être un employeur souscrivant au principe de l’égalité d’accès à l’emploi. Tous les candidats qualifiés seront pris en considération pour un emploi sans égard à la race, la couleur, la religion, le sexe, l’orientation sexuelle, l’identité de genre, l’origine nationale, le handicap, l’âge, l’état matrimonial ou tout autre statut protégé par la loi applicable.  Des mesures d’adaptation pour les candidats handicapés sont disponibles sur demande dans tous les aspects du processus de recrutement. Si vous avez un handicap qui nécessite une mesure d’adaptation, nous vous encourageons à contacter notre équipe d’acquisition de talents au [email protected], afin qu’IQVIA puisse soutenir votre participation au processus de recrutement. IQVIA s’engage à faire preuve d’intégrité dans son processus de recrutement et applique une politique de tolérance zéro en matière de fraude des candidats. Toutes les informations et toutes les qualifications soumises dans votre candidature doivent être véridiques et complètes. Toute fausse déclaration, présentation trompeuse ou omission importante au cours du processus de recrutement entraînera la disqualification immédiate de votre candidature, ou la cessation d’emploi si elle est découverte ultérieurement, conformément aux lois applicables. Nous apprécions votre honnêteté et votre professionnalisme. Veuillez noter qu'il est possible que nous utilisions l'intelligence artificielle (IA) dans le traitement de votre candidature. Cependant, nous utilisons l'IA uniquement pour aider notre équipe de recrutement à sélectionner ou à évaluer les candidatures, et non pas pour remplacer la prise des décisions par les membres de notre équipe. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, marital status, or any other status protected by applicable law.  Accommodations for applicants with disabilities are available in all aspects of the recruitment process upon request. If you have a disability that requires an accommodation, we encourage you to contact our Talent Acquisition Team at: [email protected], so that IQVIA can support your participation in the recruitment process. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. Please note that we may use artificial intelligence (AI) in the processing of your application. However, we only use AI to assist our recruitment team with the screening or assessment of candidacies, and not as a substitute for human decision-making. La fourchette salariale de base potentielle pour ce poste, annualisée, est de $72,500.00 - $120,900.00. Le salaire de base réel offert peut varier selon plusieurs facteurs, notamment les qualifications liées à l’emploi telles que les connaissances, les compétences, la formation et l’expérience; l’emplacement; et/ou l’horaire (temps plein ou temps partiel). Selon le poste offert, des régimes d’incitation, des primes et/ou d’autres formes de rémunération peuvent être proposés, en plus d’une gamme d’avantages sociaux liés à la santé, au bien-être et/ou d’autres bénéfices.  The potential base pay range for this role, when annualized, is $72,500.00 - $120,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and wellness and/or other benefits.

The team & the company   IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. With direct access to the world’s most comprehensive healthcare information, analytics and research resources, IQVIA Real World Solutions (RWS) experts design and deliver innovative data– and technology-enabled evidence programs to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. IQVIA RWS is a fast-growing and highly successful consultancy business, focusing upon on delivering tangible business results to our clients who are key decision-makers and business managers across the international pharmaceutical and healthcare industry.   Within the RWS group, the IQVIA Europe, Middle East, Africa (EMEA) Real World Methods and Evidence Generation (RW MEG) team is composed of around 200 highly qualified multi-disciplinary professionals from a variety of disciplines including health economics, statistics, biochemistry, and epidemiology, based in 12 geographies, with projects delivered across >50 countries.  Our clients operate in the life sciences industry, including global top 20 pharmaceutical companies, medical device, and biotech companies, as well as public health providers and regulatory authorities. They are looking for insight and evidence around the safety, efficacy, effectiveness and cost-effectiveness of health care delivery systems, medical devices, and pharmaceutical products spanning the full spectrum of therapeutic and disease areas. Our diverse mix of clients, the breadth of disease areas, as well as increasing access to novel data sources and methodologies provide a constant and rewarding challenge for our people.  For more information about our company please visit our website: https://www.iqvia.com/  Role purpose  This role will offer you the opportunity to support our EMEA Health Economics team as a Consultant Medical Writer and be part of our HTA Evidence & Strategy Centre of Excellence and Value Communications Centre of Excellence.  This role focusses on medical writing for HEOR purposes, where you will be responsible for writing tasks within HEOR projects and work with a senior team to co-manage small workstreams, project tasks and thought leadership initiatives. Typical projects include medical writing for the new EU Joint Clinical Assessment (JCA) dossier, HTA dossiers (e.g., NICE, SMC, NCPE, etc), global value dossiers, protocols and reports for literature reviews, reports for evidence synthesis and health economic modelling studies, and HEOR-focused peer-review manuscripts and conference abstracts. The audience for the project deliverables will be various life-sciences customers as well as healthcare payers, providers, and regulators. You will work within a team of highly experienced health economists and outcomes research specialists providing support across a range of HEOR projects, working in a cross-functional and cross-country project team, providing medical writing, undertaking quality control, and contributing to the management of project delivery (including guiding the work of more junior team members). The role will expose the candidate to the broad range of EMEA RWS offerings in value communications, HTA strategy and HEOR to support in business development opportunities. An ideal candidate will have a good understanding of the matrix structure typical of our clients from the pharmaceutical industry and how to successfully navigate this structure to achieve clients’ aims, as well as proven success in communicating scientific information in a strategic way to optimize a product’s access to markets and reimbursement.   Qualifications and Skills  Previous experience with medical writing is essential for the role. We are looking for proactive individuals with strong analytical and problem-solving skills. Candidates should have a strategic mindset, the ability to identify potential issues and suggest solutions. The ideal applicant should have apt interpersonal skills and the ability to establish relationships with both internal team members and clients. As such, fluency in conversational and business English is essential. The ability to demonstrate this through slide deck development, report writing, and presentations is essential.  We recruit individuals from a variety of backgrounds to join our well-rounded team. If you are motivated, have a passion for healthcare, and strong organisational skills and experience in medical writing we encourage you to apply. The list below should be viewed as a guide rather than a checklist.  ​Degree in life sciences (or related), epidemiology or health economics and policy, preferably a Master’s degree;  Significant experience in medical writing, including being the primary writer on peer-reviewed publications and HEOR study reports/protocols;  Familiarity with health economics and health technology assessment is a benefit;  Strong written and verbal English communication skills, expertise in scientific writing requirements;   Excellent Microsoft office skills (expert in use of MS Word), and high attention to detail;   Self-motivated with a strong desire to learn quickly and independently, ability to work autonomously with appropriate guidance when needed;  Strong time-management and organisational skills, and flexibility to work in a fast-paced environment;  Interest in data visualisation and presentation;  Keen to work as a member of a diverse, multi-cultural team. Responsibilities   Write high-quality HEOR study reports and protocols, HTA/GVD dossiers, manuscripts, conference abstracts;  Work with senior team to co-manage small workstreams, project tasks and thought leadership initiatives;  Conduct quality control reviews of HEOR documents and maintaining audit trails of changes;  Mentor and train less experienced Medical Writers;   Contribute to medical writing training initiatives to upskill the team and set quality standards;  Support the team’s Centre of Excellence initiatives.   Please submit your CV in English. IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

Team  IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. With direct access to the world’s most comprehensive healthcare information, analytics and research resources, IQVIA Real World Solutions (RWS) experts design and deliver innovative data– and technology-enabled evidence programs to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients.      Within the RWS group, the IQVIA Europe, Middle East, Africa (EMEA) Real World Methods and Evidence Generation (RW MEG) team is composed of around 90 highly qualified multi-disciplinary professionals from a variety of disciplines including health economics, statistics, epidemiology and data management, located across 8 geographies.     Our clients operate in the life sciences industry, including the global top 20 pharmaceutical companies, medical device and biotech companies, as well as public health providers and regulatory authorities. Our clients look for insight and evidence on the safety, efficacy, effectiveness and cost-effectiveness of health care delivery systems, medical devices, and pharmaceutical products spanning the full spectrum of therapeutic and disease areas. Our diverse mix of clients, the breadth of disease areas as well as increasing access to novel data sources and methodologies provide a constant and rewarding challenge for our people.      For more information about our company please visit our website: https://www.iqvia.com     Role overview  In this role within the EMEA RW MEG you will be producing materials and services relating to the Health Economics Outcomes Research business areas (health economic modelling, evidence synthesis, statistical analysis, health technology assessment submissions, report and publication development for value communication) that generate value for our clients. The role of the Consultant is expected to play an important role in shaping the team’s literature review offerings.   The successful candidate:  Will be involved in shaping and leading the team and offerings, working closely with the EMEA RWS Center of Excellence for Systematic Literature Review and the wider senior leadership team  Has a good understanding of systematic literature methods (e.g., Cochrane)  Can independently develop searches in various databases (e.g., EMBASE, MEDLINE, Cochrane, PubMed, etc.) and proficient in using OVID SP or another similar platform  Keeps up to date on new methodologies and HTAs requirements for systematic literature reviews and be an in-house go-to expert for the team  Has a good understand of different types of literature reviews (e.g., systematic, targeted, pragmatic, etc.)  Manages literature review projects with senior oversight  Guides the team on interpretation/qualitative synthesis of the literature review findings   Oversees literature review projects that meet rigorous HTA requirements, conducts quality control of literature review deliverables (searches, screening files, extractions, reporting)  Is a day-to-day contact with clients who will include pharmaceutical, biotechnology and medical devices companies with global and regional headquarters based in the EMEA region, and occasionally their affiliate teams, with senior oversight  Oversees the development of research questions, PICOS criteria, search strategies and literature review protocols   Contributes to business development as well as internal initiatives for the advancement of innovative methodological approaches   Collaborates with other business areas and functions of the organisation to deliver client services and support the development of new offerings  Qualifications and desired experience We are looking for a candidate with a good mix of academic and professional experience, domain experience and interpersonal skills. An ideal candidate has a good knowledge of literature review methods and has experience in conducting rigorous literature reviews in health sciences. The ideal candidate will also have a good understanding of the typical structure of our clients from the pharmaceutical industry and how to successfully navigate this structure to achieve client’s aims.   The list below should be viewed as a guide rather than a checklist. We want to prioritise recruiting candidates who will incorporate IQVIA’s value of ‘brave minds’ with their previous experience to put a personal spin on this role. If you share our passion for driving healthcare advancements through unparalleled data and have a passion for collaboration and solving complex problems, we encourage interested candidates who feel like they could be a good fit for the role to apply.  Desired skills and qualifications:   Postgraduate degree level education or higher from a relevant discipline such as health or bioscience-related, medicine, biomedical sciences, health economics, health policy, epidemiology, public health, or information science  Prior relevant experience, >2 years (such as, but not limited to experience in systematic literature reviews and/or meta-analyses)  Understanding of research principles, PRISMA principles, Cochrane guideline for SLRs, methods of the assessment of risk of bias for different study designs  Understanding of the principles of evidence-based healthcare, critical appraisal and the interpretation and synthesis of health care research   Understanding (and experience is advantageous) with the HTA agency requirements for evidence reviews and synthesis  Excellent oral and written communication skills  Accuracy, attention to detail and time management skills  An understanding of meta-analysis methods is advantageous, but not essential  Strong written and verbal communication skills with fluency in English  Demonstrable commercial awareness and thorough understanding of the pharmaceutical industry is advantageous   Proficiency in MS Word, PowerPoint, Excel  Eligibility to work in one of our office locations without visa sponsorship   Please submit your  CV in English. Our commitment to youIQVIA are committed to your professional growth in the healthcare industry. You will join a team of 90+ professionals working as subject matter experts, representing multiple disciplines, including HTA, health economic modelling, evidence synthesis, literature reviews, epidemiology, biostatistics, and data management. During the first three months new joiners will be paired with a more experienced hire in our ‘buddy’ system to offer support and advice in an informal setting.  IQVIA offers numerous training opportunities. You will have opportunities for external trainings and conference attendance aligned with business and team objectives. IQVIA also offers unlimited access to eLearning courses on LinkedIn Learning and Learning Edge as well as access to our internal training courses.  You will be rewarded with a competitive salary, bonus, and benefits. You will have the opportunity to gain invaluable and transferable experience within an innovative team spread out across the EMEA region. Your new role offers flexibility, including remote working and occasional office visits.  IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

El delegado se responsabilizará de la información y promoción de los productos de la Compañía en su zona geográfica de influencia, mejorando la experiencia del cliente, identificando necesidades críticas, y proporcionando soluciones óptimas para alcanzar los objetivos de negocio. Buscamos a profesionales que deseen incorporarse a un equipo de alto rendimiento en búsqueda continua de la excelencia y el liderazgo.Principales objetivos:• Identificar y priorizar adecuadamente oportunidades de negocio, demostrando buenas habilidades de análisis del territorio/cuenta/negocio.• Mantener una estrecha relación de colaboración con otros equipos de la Compañía para asegurarse que los planes que se elaboran sean consistentes, y puedan cubrir los objetivos del cliente y del negocio.• Implementar, evaluar y ajustar constantemente los planes establecidos para asegurarse que se cumplen los objetivos marcados, y demostrar compromiso para lograr los resultados.#LI-CES #LI-DNP IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

Type: Permanent full time Location: London Schedule: Monday – Friday, 9-5 (with some flexibility) We are looking for an experienced registered nurse to join the team in the London area. In this fantastic role, you will be responsible for supporting multiple patient services and healthcare professionals across various clinical settings. This position offers a diverse range of tasks/responsibilities that keep each day fresh and exciting. You will be carrying out home visits to support patients with self-injections or venepuncture, as well as setting up infusions and running clinics. There may also be some working from home supporting patients support lines. You will manage your own caseload and travel around a given geography to see patients. We offer a great range of benefits, which include: Company car plus paid mileage.Access to learning and career development tools.Annual paid holidaysNo bank holiday, weekend or evening work.Option to buy an extra 5 days of annual leave.Private healthcare (BUPA) and a competitive pension scheme.Flexible benefits, including life assurance, group income protection, personal accident insurance, dental, and wellbeing schemes for you AND your family.24/7 online wellbeing support, alongside access to learning and career development tools.Exclusive corporate rates for gym memberships and access to numerous restaurant/store discounts.We are looking for: Registered General Nurse.Proficient in phlebotomy, cannulation/ infusion experience is preferred but not essential. Training will be givenAbility to manage workload independently, meeting deadlines effectively.Good IT skills.Excellent communication skills in all formats, including face-to-face and virtual interactions.A full driving licence and flexibility for travel.IQVIA, a leader in delivering nurse programs for over 30 years, is offering an exciting opportunity for nurses seeking new careers or job growth in the UK. We collaborate with major pharmaceutical companies and the NHS directly, working on diverse disease areas and delivering over 150 successful programmes. We value diversity and inclusivity at IQVIA. If you don't meet every single requirement listed but are excited about this role, we encourage you to apply. You might be the perfect candidate for this position or another opportunity within our company! Don't miss this excellent chance to make a difference in healthcare. APPLY NOW! Please note: Sponsorship is not available for this opportunity.Candidates attend interviews at their own cost. Unfortunately, expenses incurred to attend an interview are not covered by IQVIA #LI-DNI #LI-CES #LI-WB1 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewConduct testing activities in CDMS environment and provide comprehensive testing expertise to the team to produce efficient, quality database that meets customer requirements. Essential Functions• Independently conduct testing activities to validate edit checks, system settings, SAS listings, Transfer Programming and custom reports in platforms including, InForm, RAVE, OCRDC.• Solid understanding of database structure.• Ensure validation processes and best practice guidelines are being followed strictly by self and team.• Solid understanding of documentation requirements and update all relevant documentation in a timely manner.• Communicate status of project to Validation Team Lead/Manager.• Escalate problems to the attention of Validation Team Lead/Manager.• Mentor Associate Validation Analysts in all testing activities.• Conduct Quality Reviews of testing projects on an ongoing basis as applicable.• Provide suggestions for continues process improvement and actively participate and contribute towards process improvement initiatives as assigned.• Understand and comply with core Operating Procedures and Work Instructions (including Best Practice and Guidance documents).• Meet project objectives as assigned by Validation Team Lead/Manager.• Develop and maintain good communications and working relationships with multiple teams across locations. Qualifications• Bachelor's Degree Bachelor in Science/Computer science/Information Technology or Bachelor in Technology  Req• 1 - 2 years of relevant clinical DB Testing experience in CDMS Platforms and total exp being 2+ yrs Req IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewUnder guidance, the Data Analytics Analyst performs data analysis activities to address business problems and generate insights that support decision-making. The role involves working with datasets, validating data quality, and supporting internal teams and client engagements within the healthcare and pharmaceutical domain.Job ResponsibilitiesPerform quantitative and qualitative data analysis to support internal projects and client engagementsIdentify, analyze, and interpret trends or patterns in complex datasetsCreate specifications for reports and analyses based on business requirements and available dataGenerate datasets and reports using IQVIA tools and other data platformsValidate data for accuracy, completeness, and consistencyCleanse, transform, and manipulate data to optimize analytical outcomesConduct data quality assessments and ensure data integrity across datasetsPerform audits on own work or team outputs to ensure adherence to established standards and proceduresSupport data validation, trend analysis, and inquiry resolution using standalone or enterprise systemsCollaborate effectively with cross-functional teams to meet project goalsSupport continuous improvement in data processes and analytical methodsRequired Experience and QualificationBachelor’s degree in a relevant field (e.g., Data Analytics, Statistics, Computer Science, or related discipline)1–3 years of professional experience in data analytics, preferably in pharmaceutical or healthcare dataStrong knowledge of data analysis techniques and methodologiesProficiency in Microsoft Office tools (Excel, PowerPoint, Word, Access)Experience working with SQL databases for querying and data extractionHands-on experience in data manipulation, data processing, and data validationUnderstanding of business processes and ability to translate data into actionable insightsStrong organizational and time management skillsAbility to work collaboratively across teams and functionsSkills and CompetenciesData AnalysisData ManipulationData ProcessingData CleansingData AggregationData ETL (Extract, Transform, Load)Data Quality AssessmentsData IntegritySQL DatabasesAnalytical ThinkingTime ManagementAttention to DetailCollaboration and Communication SkillsBonus (Good to Have)Experience with Python or other programming languages for data analysisExposure to pharmaceutical or healthcare datasets and domain knowledgeFamiliarity with enterprise data systems and reporting toolsUnderstanding of industry trends and marketplace dynamicsExperience in advanced data visualization or reporting toolsIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Site Enrollment and Engagement Leads collaborate with research staff and other stakeholders to drive trial recruitment and support study-specific training needs. The role acts as a strategic partner to both external and internal stakeholders to optimize the site experience and performance. They lead relationship management and communication of medical and scientific information with healthcare providers and caregivers. Essential FunctionsWorks with research sites to develop study-specific action plans to accelerate recruitment or support study-specific procedure training Provides education to healthcare professionals and their staff, reinforcing study protocols as related to a clinical trial May partner with referral networks to identify potential subjects for a trial Maintains and analyzes customer records to customize strategies to maximize pre-screening, screening, and enrollment in trials Completes internal electronic reporting systems; organizes and holds group events to optimize program delivery Successfully manages objections raised Maintains up-to-date technical knowledge of specialty and disease areas QualificationsBachelor's Degree in Health Sciences or related field, or equivalent professional qualifications Clinical research experience at the site level required Nurse or other healthcare professional preferred CRA experience preferred High flexibility to travel (internationally, if needed) Prior experience in Idiopathic Pulmonary Fibrosis and/or Pulmonary Arterial Hypertension (IPF/PAH) is a must Excellent interpersonal and communication skills Strong written and verbal communication skills, including good command of English Ability to execute tasks with minimal oversight Ability to coordinate and complete activities across multiple functions Solutions-based approach to problem-solving Positive, can-do attitude Strong customer service orientation Collaborative mindset and team player Demonstrates empathy and awareness of cultural differences Upholds the values of IQVIA IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The Assoc Dir, Linux/Unix Admin role is responsible for the management and support of the Linux and Unix servers under the management of the IQVIA CIO Cloud Services organization. This includes OS installation, configuration, upgrades, patching, backup and recovery, disaster recovery, migrations, monitoring, and performance tuning both on-premise and in cloud environments. The role is also responsible for working with internal and external customers in support of the environment. The ideal applicant should be a self-starter with a sense of ownership and have demonstrated experience in a 24/7 global environment working with other teams across the globe.Required Experience:• BS or MS in Computer Science or related major / or 10+ years relative working experience• 10+ years of experience in Managing Linux and Unix platforms.• 5+ years in a management role with multiple reports, extensive team lead experience could also be considered if right fit• Experience maintaining shift and on call rotations• Must possess good knowledge of Red Hat/Oracle Linux fundamentals and troubleshooting.• Must possess good knowledge on LVM concepts on creation, expansion and removal.• Good knowledge of networking concepts and troubleshooting• Must be conversant with storage related tasks related to Linux and VMware.• Moderate knowledge of remote management such as iLO, idrac, performing firmware updates, etc.• Knowledge of vCenter usage for performing VMware related tasks/activities such as snapshots, vMotions, etc.• Conversant with patching methodologies and procedures - knowledge of spacewalk preferable.• Basic knowledge on databases concepts preferably Oracle and MySQL and PostgreSQL.• Experience with Oracle RAC, ASM from server configuration side preferred• Knowledge of backup functionalities such as IBM's TSM, Actifio and/or Commvault for client-side administration and troubleshooting.• AIX, HP-UX and Solaris experience a plus.• Must be capable of conducting RCA for repeated incidents.• Good knowledge of ITIL concepts, prioritizing tickets, dealing with SLA, etc., ITIL certified is preferred.• Should be willing to work on 24/7 shifts and handle on call.• Strong interpersonal skills and communication is a must.• Docker/Kubernetes knowledge a plus• DevOps mindset to includer Puppet, Foreman, ansible automation.• Exposure in foreman, puppet, git, jenkins, spacewalk, collaboration, ansible, kickstart• Cloud experience (Azure is a plus)Responsibilities:• Execute & manage daily (24x7) Linux and Unix systems administration operations, including routine operations and maintenance, Incident Management, Problem Management, Change Management, Crisis Management & Disaster Recovery across multiple technologies & teams to deliver high quality & stable services.• Manage IT operational support team while complying and meeting company standards, contractual requirements & deliverables• Manage technology projects, including working with multiple vendors and company resources to deliver projects on-time and within budget• Develop & implement plans & objectives for the team in an effective & innovative fashion• Manage infrastructure operations environment and system availability for both physical and virtual Linux, Unix, and clustered environments.• Drive customer engagement and satisfaction with all support teams• Manage audit and security responsibilities that include routine reviews and reporting of technology policies and security compliance.• Develop strategies to maintain and support all servers with a goal to maximize availability and uptime.• Maintain and improve best practices and standardize processes across the Linux team.• Identify opportunities for operational efficiency through innovation and integration.• Manage and contribute to data migration projects.• Manage the team(s) and help them to achieve high levels of operational excellence.• Perform regular performance reviews of, and goals setting for, staff members.• Author SOPs, configuration specifications and related technical documentation.• Partner with the business units to develop effective solutions that solve business challenges• Mentor and train all members on team on support and troubleshooting. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Overview Provide support and assistance to project managers and project teams related to the assigned project(s). Will support all project-related activities for assigned projects in accordance with SOPs, policies and practices. Essential Functions Assist with the establishment of new procedures and offer suggestions for process improvements for existing procedures.Set up and maintain all project documentation files and records.Assist with the creation and coordinate all information and communications for assigned projects.Update and maintain internal databases, tracking systems and project plans with project specific information.Prepare, analyze and distribute status, tracking and project finance reports.Prepare presentation materials for meetings and project summary data.Coordinate project team and customer meetings, identifying and planning appropriate medium (Web, telecon, face to face) and ensuring arrangements are handled appropriately. Determine and plan all meeting requirements in advance, as directed by the Project Manager.Take and record minutes, notes and actions at assigned meetings, distribute and follow up accordingly.Coordinate with other project support staff within and across the organization to identify and consolidate support processesCoordinate the filed visits with your line managerWill serve as backup contact for internal project team as designated by project manager.Will undertake project management activities as directed by project manager.Qualifications Graduate degree in healthcare, Pharma or any medical backgroundFluency in Arabic and English is a mustHave a background about UAE charities2-3 years of related work experienceEquivalent combination of education, training and experienceGood communication and interpersonal skillsGood problem-solving skillsStrong organizational skillsResults and detail-oriented approach to work delivery and outputAbility to work under close directionStrong software and computer skills, including MS Office applicationsAbility to prioritize, actively seek input and problem solveAbility to work independently and manage time efficientlyAbility to establish and maintain effective working relationships with coworkers, managers and clientIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward. Role Overview Our Client Partner team operates at a global scale, supporting IQVIA’s strategic clients in their asset development and commercialization. Responsible for fostering strong relationships with the most senior stakeholders in the client organization, their focus is on designing and delivering integrated solutions across Consulting, Analytics, Medical Affairs, Real World Evidence, and related services. They collaborate closely with the rest of the Global Account team and Account leads from multiple service teams of IQVIA to advance client accounts in line with both immediate priorities and long‑term strategic vision. This role will operate across the client organization, particularly with senior global stakeholders in the franchise and functional teams to define and execute our priorities that move the client business forward, providing the conduit between the client and the rest of IQVIA. Responsibilities Build and nurture relationships with key executives and decision-makers within a dedicated large Pharma Account Engage with these senior stakeholders with gravitas, challenging them to think differently and providing new perspectives on their Asset Strategy Drive overall business growth globally with a focus on increasing revenue, opening new business streams and deepening our footprint in the assigned global account and assigned target assets. Lead the development of the Commercial & Medical Affairs account asset strategy with input from the broader account aligned team and orchestrate the operational execution including selection and planning around assets. Be the internal expert on the client’s priority assets with deep understanding of its market, opportunities and risks. Align the account asset strategy with RDS & RWE to ensure a joined up ‘Molecule to Market’ engagement. Build long term relationships with asset and brand leaders within the client to ensure long term revenue growth for Commercial (inc. Analytics Solutions, Consulting, RWE & Appropriate Technology). Influence the client’s strategy and position IQVIA through thought leadership and innovation aligned to client strategic asset priorities. Leverage senior IQVIA resources and subject matter experts as needed in building preferred supplier relationships. Proactively engage client asset and brand teams by anticipating client needs and leveraging the IQVIA Commercial expertise to develop both short- and long-term cross functional solutions. Lead the Commercial go to market community for headquarters or global buying centers in areas such as Commercial Consulting, Analytics Solutions, RWE-C, Advanced Analytics etc. Our Ideal Candidate The successful candidate will have a track record of success across most of the following competencies: 15+ years’ combined experience in Strategy Consulting, with a deep understanding of client engagement and solution delivery and/or; in the Pharma & Life Sciences commercial domain, with a deep understanding of business strategy and the processes of major pharmaceutical companies Demonstrated success managing a balanced pipeline of short-term tactical opportunities and long-term strategic engagements, consistently exceeding ambitious sales targets across both single‑year and multi‑year deals. Natural influencer, builds relationships easily. Excellent consultative selling skills and ability to understand client needs and pull together cross functional teams to build a compelling solution. Ability to engage with Senior Executives at client site (preferred) and remotely. Expertise in building tailored and bespoke solutions for clients and crafting a compelling story; and generating big ideas that address significant client needs. Collaboration and influence and persuasion skills. Ability to navigate and operate well within a complex matrix environment. Experience selling and negotiating large-scale and / or cross-functional solutions. Brings Excellent communication, organizational skills, logical thinking, and problem-solving capabilities. Why Join? You can drive your career at IQVIA and choose the path that best defines your development and success. With exposure across diverse geographies, capabilities, and vast therapeutic and information and technology areas, you can seek opportunities to change and grow without boundaries. We know that meaningful results require not only the right approach but also the fitting personality. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. It is an exciting time to join and reimagine what's possible in healthcare. Moving healthcare forward. Together. IQVIA is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $168,600.00 - $469,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Essential FunctionsManage about 1 local Prime site，6 other strategic sites which may locate in the other cities. Works under moderate supervision to develop new alliance site and maintain the cooperation.Support implementation of the IQVIA Prime Site strategy, works under moderate supervision to maximize site productivity, concentrating on recruiting more patients from fewer sites whilst maintaining high quality standards.Support the enhancement of the experience of patients, site staff and customers working with IQVIA through Strategic Sites.With guidance, implement the IQVIA Prime Site strategic plan promoting growth and differentiation, working with the site to execute the strategic imperatives of the plan. This will include site non-project specific strategies e.g. study start up processes, patient recruitment methodologies, infrastructure and capabilities enhancement, strengthening and alignment of recruitment pipelines and leveraging innovation to advance clinical research.Maintain and share metrics as well as pipeline information with the prime sites on a routine basis.Support identification of opportunities for Strategic Sites to participate in studies that match site capabilities, by collaborating with therapeutic area/project strategy teams. Work to adjust prime site capabilities to IQVIA available study portfolio, actively liaising with internal and external stakeholders.Be the point of contact for Governance teams, senior stakeholders and site staff. Participate and organize Joint Executive Steering Committee (JESC) and Joint Operational Steering Committee (JOSC) meetings.Collaborate with other IQVIA team members, working with the Strategic sites, to overcome any site related barriers and challenges that affect the ability of the site to produce quality project deliverables in an effective, efficient and timely manner.Share information and provide efficient communication with delivery teams, resolve site issues that have been escalated by the CRA or project teams.Ensure IQVIA processes integrate with those of the site. Support adoption of IQVIA systems by sites, or with support, create and execute guidance and solutions for internal teams when this is not possible.Mentor and support CRAs working within the Strategic Site, share best practices and lessons learned regarding site relationship management.Perform other duties as assigned.QualificationsBachelor's Degree Preferably in a scientific or healthcare disciplineTypically 5+ years of clinical research experience (e.g., CRA, SSU, PM, site-facing roles)Hands-on site interaction experienceStrong communication and coordination skillsProblem-solving and ownership mindsetDemonstrates interest in long-term site partnershipDemonstrates understanding of site relationship to business impact (preferred)IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Descripción del PuestoEnsamblar kits de prueba de laboratorio para que los investigadores los utilicen en la recolección de datos de participantes en ensayos clínicos.Producción de armado de kits, mantenimiento de entregables a los sitios y seguridad del paciente.El trabajo se realiza de acuerdo con la Guía ICH E6 de Buenas Prácticas Clínicas. Funciones Esenciales Ensamblar kits de prueba con materiales para la recolección de muestras según el protocolo. Ensamblar manuales de instrucciones para investigadores y diagramas de flujo. Empaquetar los kits de prueba completos, la documentación requerida y los materiales auxiliares necesarios, como materiales para el envío de devolución y suministros a granel, para su envío a los investigadores. Preparar paquetes para su envío. Informar al supervisor cuando los suministros estén por debajo del nivel de inventario requerido para evitar retrasos en el inicio del estudio y en los requerimientos de reabastecimiento. Mantener un área de trabajo limpia y ordenada. Requisitos Título de colegio secundario o equivalente (Requerido). 1-2 años de experiencia relevante. Atención al detalle. Buena capacidad de lectura. Conocimientos básicos de informática. Excelentes habilidades organizativas. Capacidad para establecer y mantener relaciones laborales efectivas con compañeros, gerentes y clientes. Disponibilidad para trabajar de forma presencial todos los días en la oficina (Ubicación: Villa Ortúzar, CABA). Dentro de CCT de comercio. #LI-NRJ #LI-Onsite IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Overview The Specimen Receipt and Processing Associate is responsible for assisting with a variety of routine activities associated with receipt of clinical specimens. Essential Functions • Responsible for assisting with receipt of consignments and shipments • Responsible for the opening of shipments and the quality check of patient info forms. Escalates incorrect,missing information, or damaged shipments to senior level staff • Responsible for correct disposal and/or recycling of kit shipping supplies • Ensures specimens are not left in kit packaging by conducting a secondary check of shipping materials. • Supports and responds to after-hour alarms and/or other job critical functions. • Assists in maintenance of equipment. • Assists with supply inventory functions and general clean up of workstations. • Performs various administrative duties as required. • Responsible for organizing the work area, as requested by management. • Dependent upon functional area, may also handle receipt of compounds and control material. • Responsible for following safety procedures. • Participates in continuing education through self study and attendance of meetings. • Performs work in accordance with company procedures and applicable regulatory guidelines. Qualifications • High School Diploma or equivalent • Basic Computer skills. • Ability to maintain effective reporting procedures and control workflow. • Ability to establish and maintain effective working relationships with coworkers, managers and clients. Please note that this role requires on-site work from Tuesday to Saturday. Working hours to be confirmed. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Location: South West England & South Wales We are working with a pharmaceutical company focused on improving care for patients with ADHD. They are looking to appoint a Key Account Manager to cover South West England and South Wales. The role This is a field based position with responsibility for managing a broad and strategically important territory. You will work across primary and secondary care, engaging with healthcare professionals involved in the diagnosis and management of ADHD. The role focuses on key account management, with an emphasis on identifying areas of opportunity, maintaining existing relationships, and supporting appropriate patient access to treatment. You will be responsible for planning and managing your territory, using available data and insight to prioritise activity and support business objectives. Responsibilities Develop and maintain territory and account plans aligned to business prioritiesBuild and maintain relationships with relevant healthcare professionals and stakeholdersIdentify opportunities within key accounts to support appropriate patient accessDeliver accurate and compliant clinical and commercial informationReview territory performance and use data to inform activityWork with internal colleagues to support a consistent approach across accountsAbout you Experience in pharmaceutical, healthcare or medical salesUnderstanding of working within a field based roleAble to plan and manage a territory effectivelyComfortable working independently across a large geographical areaAble to engage with a range of healthcare stakeholdersOpen to feedback and ongoing developmentFull UK driving licenceAbout the role and team Established territory with existing customer relationships in placeStructured support including account planning, data insights and materialsCoaching led management approach with regular communication and supportOpportunity to take ownership of how you manage and develop your accountsPart of a growing organisation within a developing therapy areaWhat is offered Opportunity to manage an established ADHD portfolioHigh level of ownership within the roleSupportive team environmentSalary and benefits aligned to experiencePlease note this role does not support sponsored visa's#LI-DNI #LI-CES #LI-SP1   IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Financial Analyst – Business Operations Support About the Role  This role sits within the Global Procurement and Travel & Payment Solutions team and acts as a hybrid between Finance, Operations, and Customer Support. The role serves as a key connector (‘glue’) between global travel programs, payment solutions, and IQVIA Concierge Travel Services (ICTS).  Key Responsibilities  Perform financial postings, reconciliations, and journal entries in ERP systems (SAP, PeopleSoft)  Reconcile high-volume transaction data (e.g., airline tickets, meetings & events spend)  Manage and analyse virtual credit card transactions and payment flows  Prepare cost breakdowns and financial summaries for meetings, travel, and events  Support global travel program and payment solutions operations  Interact with internal stakeholders (from operational level to senior leadership) to resolve queries  Support ICTS team with financial processes related to meetings and events  Own and resolve data discrepancies proactively   Automation & Data  Identify opportunities to automate repetitive processes  Build solutions using Power Automate, Copilot, or similar tools  Lverage Excel and Power BI for data analysis and reporting   Tools & Systems  SAP, PeopleSoft (ERP)  Excel (advanced)  Power BI (preferred)  Power Automate, Copilot, Cursor (or similar automation tools)  Coupa, Concur (Expense & Booking)  Citibank / American Express platforms   Profile  3+ years in finance / accounting / shared services  Strong Excel and data handling skills  Experience with ERP systems and reconciliation processes  Strong communication and customer-facing mindset  Proactive, independent, problem-solving attitude IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is 18.900,00 € - 28.300,00 €. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Site Activation Specialist Country Site Activation - CSA Serbia Homebased Make an impact on patient health! IQVIA’s Global Site Activation Team of 2000 employees, drives best in class site and customer experience, with industry leading outcomes. We keep the patient at the forefront; ‘Always Impatient for the Patient’ and we excel in our collaboration with our external/internal customers. IQVIA’s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication. We are leaders in innovation and first to new technologies, meaning a vast amount of career development opportunities are available. Job Overview: As a Site Activation Specialist, you will serve as a Single Point of Contact to perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager, Project Management team, and other departments as necessary. You will be responsible for regulatory submissions for UK and Ireland. You will review documents for completeness, consistency, and accuracy, under guidance of senior staff and prepare site documents, inform team members of completion of regulatory contracts. Along with distributing completed documents to sites and internal project team member and updating and maintaining internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project specific information. You will also review, track, and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form, and Investigator Pack release documents. Requirements and Skills : Bachelor’s Degree in Life Science 2 - 3 years’ prior experience in clinical research / site activation Experience of regulatory submissions essential. Ability to work independently but also collaborate with others Leadership skills Good interpersonal, communication and organisational skills to establish and maintain effective working relationships with co-workers, managers and sponsors Ability to work on multiple projects Knowledge of applicable functional/regulatory requirements, including local regulations, SOPs and ICH/ GCP Join IQVIA and let’s create a healthier world together: Exposure across 21 Therapeutic Areas Be part of a global team who operate across 141 locations Exposure across a variety of studies and projects Access to new, innovative technologies Work within a collaborative and vibrant environment Own your career! Unleash your potential! It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world. When you join our diverse, global team, you’ll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Senior Site Activation Coordinator Country Site Activation – CSA Serbia Homebased Make an impact on patient health! IQVIA’s Global Site Activation Team of 2000 employees, drives best in class site and customer experience, with industry leading outcomes. We keep the patient at the forefront; ‘Always Impatient for the Patient’ and we excel in our collaboration with our external/internal customers. IQVIA’s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication. We are leaders in innovation and first to new technologies, meaning a vast amount of career development opportunities are available. Job Overview: As a Site Activation Coordinator, under general supervision, you will perform tasks at a country level associated with site activation activities. These activities will be in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. You will perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs, and work instructions, working closely with the Site Activation Manager, Project Management team, and other departments as necessary. Coupled with reviewing documents for completeness, consistency, and accuracy, under guidance of senior staff, you will prepare site documents, review, track and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form, and Investigator Pack release documents. You will also support the updating and maintenance of internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project specific information. Requirements: Bachelor’s Degree in Life Science or related field Minimum 2 years’ work experience; 1+ years in healthcare or similar Good interpersonal, communication and organizational skills to establish and maintain effective working relationships with co-workers, managers and sponsors Ability to work on multiple projects Join IQVIA and let’s create a healthier world together: Exposure across 21 Therapeutic Areas Be part of a global team who operate across 141 locations Exposure across a variety of studies and projects Access to new, innovative technologies Work within a collaborative and vibrant environment Own your career! Unleash your potential! It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world. When you join our diverse, global team, you’ll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

experimental execution in support of sample analysis and validation.  Responsible for root cause analysis, troubleshooting, and supporting process improvements. Essential Functions• Responsible for performing and documenting analytical procedures in accordance with company procedures and regulatory guidelines.• Assists in troubleshooting and process improvements to increase data quality, lower costs, or reduce turnaround times to include, updating standard procedures, assisting with troubleshooting.• Acts as a technical resource for laboratory staff and support the team in the absence of the line manager.• Performs routine data analysis to determine if an analytical procedure is proceeding according to expectations and that the results are within acceptable tolerances.• Identifies and documents potential performance errors or otherwise unusual results and escalates to senior lab personnel.• Prepares data analysis results for upload to LIMS system under the guidance of senior level staff.• Contributes to CAPA investigations, deviations, and resolution.• Responsible for clear, accurate, and timely communications with cross functional stakeholders.• Assists in maintaining laboratory equipment and may offer suggestions for new equipment.• Assists in good housekeeping of the lab environment, consistent with 6S standards.• Assists in maintaining adequate inventory.• Responsible for preparation of buffers and solutions for analysis, as required.• Performs and documents calibration and maintenance of laboratory equipment as assigned.• Performs and documents hands on training for other lab personnel in areas of proven competency as assigned.• Participates in continuing education through self-study, attending training sessions and  lectures and meetings.• May lead a laboratory or cross functional projects and assist with implementation of changes.• May be responsible for contributing to the design and development execution of routine methods/assays under moderate supervision.• Supports safety, quality, and 6S requirements and initiatives.• Complies with company's procedures and applicable regulatory requirements. Qualifications• Bachelor's Degree Bachelors Degree Or equivalent combination of education and experience (Some CAP/CLIA lab locations may require a BSc in in a chemical, physical, biological or clinical laboratory science, medical laboratory technology or cytotechnology.)  Req• Typically requires >2 of experience. Req• Minimum 1 year of experience in a regulated laboratory environment preferred. Pref• Sound knowledge of principles, theories, and concepts in job area.• Working knowledge of any applicable regulatory standards within area of responsibility.• Proficiency with relevant laboratory techniques.• Knowledge of laboratory safety and infection control procedures and practices including standard precautions and hazardous chemical handling ,• Strong technical knowledge of complex testing procedures and science supporting the analysis.• Proficiency with complex laboratory calculations regarding batches and specimens.• Ability to troubleshoot laboratory equipment and resolve process issues.• Good computer skills including proficiency with Microsoft Excel, PowerPoint and Word.• Effective organizational and interpersonal skills.• Effective communication and presentation skills.• Capable of handling multiple tasks simultaneously.• Strong attention to detail and accuracy.• Ability to establish and maintain effective working relationships with coworkers, managers and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

【工作职责】 1. 参与卫生经济学评价、卫生技术评估、价值沟通、疾病负担研究、价值沟通、定价与准入政策及策略分析方面的项目； 2. Desk research，包括文献检索与公开信息收集； 3. 协助开展专家访谈； 4. 支持卫生经济学Excel分析模型搭建； 5. 统计分析、PPT制作与报告撰写等。 【任职要求】 1. 就读于国内外优秀高校的在读硕士或博士生; 2. 公共卫生、卫生经济学、流行病学、临床医学、医学统计学等相关专业背景优先； 3. 有咨询行业实习经验或相关研究经历的优先； 4. 中英文听说读写流利； 5. 有责任心，工作细致认真，抗压能力强 6. 能够熟练使用Office软件（Excel, PowerPoint, etc.）及统计分析软件； 7. 每周至少工作3天，可全职工作者优先考虑，持续3个月或以上。 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.