IQVIA

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.

The AI Security & Governance Architect is a senior individual contributor role within IQVIA’s Security Architecture team. Artificial intelligence and generative AI are transforming how IQVIA operates — from developer productivity and business workflows to data analytics and clinical innovation. As adoption accelerates across the enterprise, the security organization must scale its ability to govern, assess, and enable that adoption responsibly and at pace.This role sits within a broader AI security strategy function and reports to the Security Architecture leader responsible for IQVIA’s enterprise AI security direction. The AI Security & Governance Architect is instrumental in executing and maturing that strategy: working directly with development teams, the Data Office, and business units across IQVIA’s global operations to embed security and governance into AI adoption — asking the right questions, establishing the right workflows, and maintaining the visibility and control the organization needs as AI use scales.IQVIA has existing AI governance committees and taskforces in place. This role is not a greenfield build, but the pace of AI adoption across the business demands a significant step-up in program maturity, coverage, and consistency. The AI Security & Governance Architect will be central to that effort — owning key governance and assessment workstreams, representing Security Architecture in cross-functional forums, and ensuring that as IQVIA scales its use of technologies such as Microsoft Copilot, Claude, and other leading generative AI platforms, it does so with the appropriate security controls, governance frameworks, and architectural guardrails in place.You will sit within the global Information Security organization, with close working relationships across Security Architecture, Cloud Security, Application Security, the Data Office, Legal, Privacy, Compliance, and business units spanning IQVIA’s global operations. Principal responsibilities will include: •    Contribute to and help execute IQVIA’s AI security strategy, providing hands-on program delivery across governance, risk assessment, and stakeholder engagement workstreams under the direction of the Security Architecture AI lead.•    Act as a primary security architecture partner for business units, development teams, and the Data Office as they evaluate, adopt, and scale generative AI tools and platforms — including productivity and developer assistance tools, enterprise AI platforms, and AI-enabled workflows — ensuring security requirements are understood and addressed from the outset.•    Own and operate the AI security intake and review process for new generative AI platform and tool requests, conducting structured security assessments that evaluate vendor security posture, data handling and residency practices, telemetry and logging controls, and acceptable use implications before organizational adoption is approved.•    Represent Security Architecture in IQVIA’s existing AI governance committees and taskforces, ensuring security risk positions, architectural guardrails, and governance requirements are embedded in decisions and communicated consistently across the organization.•    Develop, maintain, and operationalize AI security standards, guidelines, and reference architectures covering generative AI platforms, LLM-integrated applications, agentic systems, and AI-enabled developer and productivity tooling.•    Conduct AI security architecture reviews for new and existing AI integrations, including agentic workflows, retrieval-augmented generation (RAG) pipeline designs, LLM API integrations, and multi-model orchestration patterns — identifying risks and defining appropriate mitigations in collaboration with development and platform teams.•    Build and maintain scalable AI security workflows, assessment playbooks, and decision frameworks that enable the organization to evaluate AI adoption requests efficiently, consistently, and without creating unnecessary friction for business delivery.•    Define and maintain security requirements for enterprise generative AI platforms, addressing prompt security, data residency, access and identity controls, output handling, audit logging, and integration with IQVIA’s broader identity and data governance controls.•    Partner with development teams to provide practical AI security guidance, supporting the secure design of AI-integrated applications and ensuring development teams have the guidance, patterns, and standards needed to build responsibly with AI technologies.•    Support the development of AI security awareness and guidance materials for developers, data teams, and business stakeholders across IQVIA, ensuring consistent understanding of how AI tools should be used within IQVIA’s security and governance framework.•    Monitor the evolving AI security and regulatory landscape — including emerging attack techniques, model provider disclosures, and developments in AI regulation — and translate findings into timely, actionable updates to IQVIA’s AI governance posture and security standards.•    Collaborate with Legal, Privacy, and Compliance teams on AI-related regulatory requirements, including obligations under the EU AI Act, GDPR implications of AI data processing, and sector-specific requirements applicable to life sciences and healthcare AI deployments.•    Define metrics and reporting for AI security governance, providing CISO leadership and governance stakeholders with clear visibility into AI adoption volume, risk profile, assessment coverage, and program maturity across the organization. Required Experience and Qualifications •    Substantial progressive experience in Information Security, Security Architecture, or related technical roles, with demonstrated expertise in AI security, cloud security, or application security.•    Strong working knowledge of generative AI security risks and controls, including prompt injection, data leakage, model abuse, output manipulation, and the supply chain and integration risks associated with third-party AI platforms and APIs.•    Experience assessing and governing the adoption of enterprise AI and generative AI tools, including productivity platforms such as Microsoft Copilot, developer assistance tools, and LLM-integrated applications and workflows.•    Familiarity with AI security frameworks and standards including OWASP LLM Top 10 and NIST AI RMF, and working awareness of EU AI Act obligations relevant to enterprise AI governance and security.•    Experience engaging with governance committees, risk review boards, or cross-functional taskforces as a security subject matter expert, influencing decisions and representing security requirements to non-security stakeholders.•    Working knowledge of cloud environments (Microsoft Azure and/or Amazon AWS) and the AI and ML services offered within those platforms, with the ability to assess security configurations, data handling behaviors, and integration risks.•    Experience partnering with development teams, data teams, and business stakeholders to translate security and governance requirements into practical, delivery-compatible guidance and standards.•    Strong understanding of data protection principles as they apply to AI systems, including data residency, purpose limitation, PHI and PII handling in AI workflows, and cross-border data transfer implications under GDPR and applicable regional regulations.•    Familiarity with secure architecture patterns for LLM-integrated systems, including RAG pipeline security, agentic system design, prompt workflow controls, and API gateway patterns for model endpoints is preferred.•    Experience within regulated industries — life sciences, healthcare, or financial services — with awareness of sector-specific compliance and data protection obligations relevant to AI use is preferred.•    Bachelor’s degree in Computer Science, Information Security, or equivalent practical experience is preferred.•    Relevant certifications such as CISSP, CISM, CCSP, AWS/Azure Security Specialty, or equivalent are preferred but not mandatory.•    Strong written and verbal communication skills in English, with the ability to produce governance documentation, security standards, and executive-level reporting across a global, matrixed organization. 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.

Software Developer / Application Developer (m/w/d) – Schwerpunkt Datenbank & Backend - C++/PHP (m/w/d) full remote Leipzig / Vollzeit (in Gleitzeit) Health System Services (HSS) wurde 1990 gegründet und ist einer der führenden Technologieanbieter und Dienstleister im deutschen Gesundheitsmarkt. Zu den Schwerpunkten unserer Tätigkeit gehören das Genehmigungs- und Abrechnungsmanagement, die Softwareentwicklung und -bereitstellung sowie Digitalisierungs- und Archivierungsleistungen für Krankenkassen. Deine Aufgaben Entwicklung, Pflege und Optimierung von Anwendungen im Bereich Datenmanagement Umsetzung von fachlichen Anforderungen in technische Lösungen (Konzeption, Entwicklung, Tests) Entwicklung und Anpassung von Prüfalgorithmen in Datenbanken Arbeit mit C++, PHP sowie SQL-basierter Datenbankentwicklung (insb. SQL / Oracle) Pflege und Weiterentwicklung von Import- und Exportprozessen Ticketbearbeitung sowie aktive Mitwirkung in agilen Routinen (Daily, Sprintplanung) Erstellung und Pflege technischer Dokumentationen sowie Unterstützung im 3rd-Level-Support Enge Zusammenarbeit mit Team, Fachbereichen und Qualitätssicherung Dein Profil Abgeschlossenes Studium der Informatik oder eine vergleichbare Qualifikation Mehrjährige Berufserfahrung (ca. 3–5 Jahre) in der Software- oder Datenbankentwicklung   Anwendbare Kenntnisse in C++ und/oder PHP sowie Datenbanken (z. B. Oracle, SQL) Erfahrung im Umgang mit Tools wie Jira, Git, Confluence Idealerweise Erfahrung mit weiteren Technologien wie Python oder Perl Schnelle Auffassungsgabe und Freude an komplexen fachlichen Themen Verhandlungssichere Deutschkenntnisse (mind. B2/C1) Werde Teil unseres Teams und gestalte gemeinsam mit uns die digitale Transformation im Gesundheitswesen. Das erwartet Dich: Flexible Arbeitszeiten im Gleitzeitmodell und hybrid (remote und im Office), full remote / anlassbezogen im Büro Faire Überstundenregelung mit Freizeitausgleich oder einer Vergütungsmöglichkeit mit 25% Überstundenzuschlag Mentoren-Programm während deiner gesamten Einarbeitungszeit Geregelte Feedbackschleifen in der Einarbeitung ("4 Tage, 4 Wochen, 4 Monate-Prinzip") und jährliche Entwicklungsgespräche Interne Entwicklungsmöglichkeiten innerhalb des IQVIA Konzerns Individuelle Weiterbildungen, unternehmensinterne Workshops, Teilnahme an Fachkonferenzen möglich Kantine mit subventioniertem Essen (Mittagsgericht ab 1,30 €) Kostenlose Kalt- und Heißgetränke und kostenfreies Obst Betriebliche Altersvorsorge Rabatte im Partner-Reisebüro Kostenfreie und anonyme Beratung zu gesundheitlichen, familiären und rechtlichen Anliegen über Talingo Vergünstigtes LVB-Jobticket Unternehmensevents, Weihnachtsfeiern und Teambuildings Wir schätzen Vielfalt und begrüßen daher alle Bewerbungen – unabhängig von Geschlecht, Nationalität, ethnischer und sozialer Herkunft, Religion/Weltanschauung, Behinderung, Alter sowie sexueller Identität 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.

Consultant Cardiologist Location: North West England/Merseyside Join the IQVIA Healthcare Professionals Network Today! Are you a Cardiologist Consultant with proven experience in paediatric echocardiography? IQVIA is seeking skilled professionals to join our Healthcare Professionals Network and support flexible bank work opportunities in Merseyside About the Role: Perform high-quality paediatric echocardiography in line with BSE standards. Deliver accurate and timely diagnostic reports to support patient care. Work collaboratively with multidisciplinary teams in a dynamic healthcare environment. Flexible bank shifts to suit your availability. ​Why Join IQVIA Healthcare Professionals Network? Access to a wide range of flexible opportunities across the UK. Be part of a global leader in healthcare solutions. Continuous support and resources to help you succeed. Opportunities to expand your professional network and skills. #LI-CES #LI-CT1 #LI-HCPN #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

As a global leader in commercial solutions, IQVIA is uniquely positioned to deliver results both nationally and internationally. Our teams partner with biopharma companies to bring essential medicines to the people who need them most. We empower our clients with insights and access to their markets, helping them demonstrate the value of their products to payers, physicians, and patients alike. A core part of our mission includes serving as the sales force for biopharma or providing nurse educators who support patients and prescribers. With the right experience, you can help bring medical innovations to life in real-world settings. We’re excited to announce an opportunity to join our team of over 10,000 field professionals worldwide—we’re currently hiring a Nurse Educator to support our pharmaceutical and biotech clients. Nurse Educator At the heart of our business strategies is a commitment to patients. The Nurse Educator Program is a patient-centered, educational initiative designed to support individuals living with chronic conditions who have been prescribed specific therapies. Nurse Educators play a vital role in helping patients understand their treatment, manage their condition, and access relevant resources related to their prescribed medication. This role involves one-on-one engagement with patients through various channels, including in-person visits, phone calls, video conferencing, email, and SMS—always in strict alignment with program guidelines. Please note: this is an educational role only. Nurse Educators do not provide clinical care or medical advice. Role Overview: Nurse Educator As a Nurse Educator, you will play a key role in supporting patients by connecting them with program-approved resources and delivering personalized education on chronic disease management and prescribed therapies. This role is designed to empower patients, promote treatment adherence, and encourage meaningful dialogue with healthcare providers. Key Responsibilities Facilitate connections between patients and approved educational resources. Deliver direct, disease-specific education and training related to prescribed medications. Support multiple disease states and therapies as needed. Promote behavioral change through patient-centered education to improve treatment adherence. Encourage effective communication between patients and their healthcare providers. Qualifications Bachelor’s degree and/or BSN preferred. Active RN license in state of residence; compact multi-state license preferred where applicable. Nursing license must be current and in good standing. Minimum of 5 years of clinical experience in healthcare (hospital, home health, pharmaceutical, or biotech settings). Prior experience as a nurse educator is preferred. Bilingual in English and Spanish is a plus. Valid driver’s license required. Must reside within the designated territory. Experience in direct patient interaction with a focus on adherence and persistence. Strong understanding of clinical data and pharmacology. Excellent time management, planning, and multitasking skills. Effective presentation and motivational skills; strong interpersonal and communication abilities. Ability to work independently and cross-functionally. Dedicated home workspace required. Adaptability to changing responsibilities and environments. Proficiency in Microsoft Office (Word, Excel, PowerPoint) and iPad technology. Flexibility to work evenings and weekends as needed. Willingness to travel up to 60–70%. Compliance with client vaccination requirements may be necessary. Compensation Competitive annual salary Car allowance Bonus eligibility  #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 $95,000-$105,000 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.

equirements considering business and application needs.  Organizes metadata for use by teams. Essential Functions• Designs or modifies data models to solve complex database requirements considering business and application needs.  Organizes metadata for use by teams.• Plans, conducts and coordinates the design of state-of-the-art data model designs and metadata management.• Provides application-level data modeling for project development teams.• Assists with creating and maintaining enterprise-wide data standards.• Participates in enterprise-wide logical data modeling and leads efforts on assigned data subject areas.• Assists with the implementation of metadata management tools.• Facilitates formal and informal discussions to support database designs.• Participates in the implementation and management of the global metadata repository.• Identifies metadata sources, develops metadata management capabilities, monitors metadata quality, and develops common data definitions.• Coordinates testing and documentation of the global metadata repository and conducts user interviews to gather metadata requirements to insure business requirements are met. Qualifications• Bachelor's Degree Computer Science, a related field, or equivalent experience Req• Database systems knowledge with a minimum of five (5) years IT with two (2) years experience in the data administration area. 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.

La maîtrise de l'anglais et du français est requise pour ce poste. L’équipe d’activation des centres nationaux d’IQVIA constitue un réseau mondial qui identifie et active les centres de la plus haute qualité pour garantir que les patients participant aux essais cliniques ont accès à des médicaments sûrs et efficaces. Nous sommes à la pointe de l'innovation et des nouvelles technologies, ce qui signifie que de nombreuses possibilités d'évolution de carrière sont disponibles. En tant que coordinateur principal de l'activation des centres, vous exécuterez, sous une supervision générale, des tâches au niveau national liées aux activités d'activation des centres. Ces activités seront conformes aux réglementations locales et/ou internationales applicables, aux procédures opérationnelles standard (POS), aux exigences du projet et aux lignes directrices contractuelles/budgétaires. Votre mission peut également comprendre des activités de maintenance. · Réaliser des études de faisabilité, d'activation du centre et certaines activités de maintenance dans le cadre d'études assignées pour des sites d'investigation, conformément aux réglementations applicables, aux procédures opératoires normalisées et aux instructions de travail, en travaillant en étroite collaboration avec le gestionnaire d'activation du centre (GAC), l'équipe de gestion de projet et d'autres départements si nécessaire. · Examiner les documents pour s'assurer qu'ils sont complets, cohérents et exacts, sous la direction du personnel d'encadrement. · Préparer les documents du centre, en vérifiant leur exhaustivité et leur exactitude · Examiner, suivre et contrôler l'avancement, l'approbation et l'exécution des documents requis tels que les questionnaires, les CDA, les documents réglementaires, éthiques, les formulaires de consentement éclairé (FCE) et les documents de libération du dossier de l'investigateur (IP). · Informer les membres de l'équipe de l'achèvement des documents contractuels et autres documents réglementaires pour les différents centres. · Répartir les documents complétés entre les centres et les membres de l'équipe de projet interne. · Contribuer à la mise à jour et à la maintenance des systèmes internes, des bases de données, des outils de suivi, des calendriers et des plans de projet en fournissant des informations précises et complètes sur les projets. CONNAISSANCES, COMPÉTENCES ET APTITUDES REQUISES · Baccalauréat en sciences de la vie ou dans un domaine connexe préféré · Expérience professionnelle d’au moins 2 ans; 1 an dans le domaine de la santé ou similaire considéré comme un atout · Capacité à parler couramment sa langue maternelle, y compris à maîtriser l'anglais · Travaille sous supervision générale et atteint des objectifs qui ont un impact significatif sur les résultats d’un domaine de travail. · Bonne communication interpersonnelle et sens de l'organisation pour établir et maintenir des relations de travail efficaces avec les collègues, les responsables et les promoteurs. · Capacité à gérer le changement et les situations complexes · Capacité à travailler sur plusieurs projets · Connaissance générale de l'environnement des essais cliniques et du processus de développement des médicaments. · Bonnes compétences technologiques et connaissance des applications MS Office Fluency in both English and French is required for this role.   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.    As Senior 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. Your task may also include maintenance activities.    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 (SAM), Project Management team, and other departments as necessary  Review documents for completeness, consistency and accuracy, under guidance of senior staff  Prepare site documents, reviewing for completeness and accuracy   Review, track and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents  Inform team members of completion of regulatory contractual and other documents for individual sites   Distribute completed documents to sites and internal project team members  Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information     REQUIRED KNOWLEDGE, SKILLS AND ABILITIES  Bachelor’s Degree in Life Science or related field preferred   Minimum 2 years’ work experience; 1+ years in healthcare or similar considered advantageous   Fluent/ native language capabilities, including English   Works under general supervision and delivers objectives that significantly impact results for a job area  Good interpersonal communication and organizational skills to establish and maintain effective working relationships with co-workers, managers and sponsors  Ability to handle change and ambiguity  Ability to work on multiple projects  General awareness of clinical trial environment and drug development process advantageous   Good technology skills and knowledge of MS Office applications  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 $51,200.00 - $85,300.00. 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 $51,200.00 - $85,300.00. 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 wellness and/or other benefits.

Job OverviewProvide experienced technical expertise to develop process methodology for department to meet internal and external clients’ needs. Plan and coordinate the development of integrated programming solutions serving the full spectrum of statistical programming needs. Provide technical expertise and leadership to the department. Provide internal consulting services, including specifications and user needs analysis for complex project or client requirements. Essential Functions• Perform, plan and co-ordinate the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing summaries and (ii) the programming of analysis databases (derived datasets) and transfers of data for internal and external clients. May perform and plan the programming of database quality control checks.• Program and plan the integration of databases from multiple studies or sources.• Develop and co-ordinate programming documentation including plans and specifications, as appropriate, for complex studies.• Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to teams and department, for complex studies.• Perform, plan and co-ordinate the development, implementation and validation of new process technologies, macros and applications.• Fulfill project responsibilities at the level of statstical team lead for single complex studies or group of studies.• Understand the Scope of Work, budget and quote assumptions, estimate the work completed, manage Out of Scope and resource forecasts for single studies. May manage project budget and resource requirements, and provide revenue forecasts for single studies.• Provide training and guidance to lower level staff. Qualifications• Master's Degree Computer science or related field and 3 years relevant experience Req Or• Bachelor's Degree Computer science or related field and 4 years relevant experience Req• Equivalent combination of education, training and experience in lieu of degree Req• Knowledge of statistics, programming and/or clinical drug development process• Advanced knowledge of computing applications such as Base SAS, SAS Graph and SAS Macro Language• Good organizational, interpersonal, leadership and communication skills• Ability to effectively manage multiple tasks and projects• Excellent accuracy and attention to detail• 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.

Job OverviewPrepares and/or reviews regulatory submissions to support clinical trial and marketing authorisation activities for either internal and/or external clients.  Independently provides regulatory support for more complex projects. Essential Functions Acts as a Regulatory Team Leader on complex projects, which may include technical writing and/or may act as a Project Manager for a stand-alone project, with guidance from senior staff as appropriate. Competently writes regulatory and/or technical documents with minimal review by senior staff. Establishes relationships with many customers; may meet face to face without rest of team to discuss regulatory issues and present lessons learned.  Adopts a proactive and flexible approach to resolve any issues. Undertakes detailed review and management of budgets related to projects, including out of scope activities. Ensures revenue is recognised and challenges when appropriate, may seek guidance from senior staff as appropriate. May give guidance to junior colleagues, including feedback on the quality of technical documents, and may assist in their training and development. May present to clients at bid defence meetings by phone or in person, for a range of regulatory deliverables, at discretion of senior staff. May write new regulatory SOPs, and/or propose revisions and/or act as reviewer for regulatory SOPs, as assigned and appropriate. May be involved in a Regulatory and/or IQVIA Initiative. Performs other tasks or assignments, as delegated by Regulatory management. Qualifications Bachelor's Degree in Life science or related discipline Master's Degree in Life science or related discipline Demonstrates comprehensive regulatory or technical area of expertise Good negotiating skills and the ability to identify and resolve issues, using flexible adaptable approach Strong software and computer skills, including MS Office applications Demonstrated skills in chairing small meetings Ability to work on several projects, retaining quality and timelines and can prioritise workload with minimal supervision Ability to propose revisions to SOPs or suggest process improvements for consideration 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.

We are seeking Bioanalytical Automation Scientist to join IQVIA Laboratories at Durham, NC.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Job Summary:We are looking for a hands-on bioanalytical scientist eager to work at the intersection of laboratory science, automation, and digital innovation. This role focuses on executing and evolving bioanalytical workflows while translating assays into scalable, automation-ready processes. What You'll Be Doing:Execute bioanalytical workflows with scientific rigor, including method execution, troubleshooting, and optimizationTranslate assays into automation-ready steps through standardization and variability reductionPartner with engineering teams to develop automated protocols and define acceptance criteriaDrive assay robustness through effective controls, sample integrity practices, and contamination preventionUse data to identify failure modes, perform root cause analysis, and implement method improvementsContribute to documentation, deviations, CAPA inputs, and inspection readiness activitiesChampion digital data capture and support right-first-time execution practices What We Are Looking For:Bachelor’s degree in a life science discipline with relevant hands-on bioanalytical laboratory experienceExperience with bioanalytical methods, troubleshooting, and laboratory workflow optimizationExposure to laboratory automation platforms, LIMS/ELN systems, or digital data workflowsOther equivalent combination of education, training, and experience may be accepted in lieu of degree The Knowledge, Skills and Abilities Needed for This Role:Strong analytical and problem-solving skills with the ability to troubleshoot complex laboratory processesAbility to work effectively in compliance-driven environments with attention to documentation and data integrityEffective communication skills to collaborate across multidisciplinary teams including engineering and quality What We Offer You:We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey. To learn more about our benefits, visit https://jobs.iqvia.com/benefits. If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!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 $46,200.00 - $96,200.00. 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.

We are seeking Senior Automation Scientist to join IQVIA Laboratories at Durham, NC.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Job Summary:Design, build, and scale laboratory automation that advances bioanalytical ligand binding testing through robotic sample handling, automated preparation, instrument integration, and workflow orchestration. In this hands-on role, you will partner with scientists and Quality to deliver reliable, traceable, and compliant automated workflows in a regulated laboratory environment. What You'll Be Doing:Design and implement automation cells for liquid handling, robotic integration, plate movement, and barcode-enabled sample trackingIntegrate laboratory instruments with digital systems such as LIMS, ELN, scheduling tools, and data capture platformsDevelop control logic, scripts, and interfaces that support automated workflows, exception handling, and error recoveryBuild and maintain monitoring capabilities for uptime, throughput, logs, dashboards, and alertsTranslate assay steps into robust and scalable automation protocols in partnership with laboratory scientistsSupport validation documentation, audit readiness, and change control activities in collaboration with QualityDrive continuous improvement by reducing failure modes, simplifying maintenance, and improving cycle time What We Are Looking For:Bachelor’s Degree in Science/Engineering or related field required5+ years in laboratory operations, lab transformation, automation programs, or digital lab systemsHands-on experience with lab automation platforms such as liquid handlers and robotic integration systemsProficiency in scripting or programming for automation and integration using Python, C#, JavaScript, or equivalentOther equivalent combination of education, training, and experience may be accepted in lieu of degree The Knowledge, Skills and Abilities Needed for This Role:Strong troubleshooting skills across hardware, software, sensors, and laboratory processesAbility to collaborate cross-functionally and translate scientific workflows into reliable automation solutionsWorking knowledge of regulated laboratory environments with disciplined documentation practicesContinuous improvement mindset with focus on reliability, scalability, and operational efficiency What We Offer You:We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey. To learn more about our benefits, visit https://jobs.iqvia.com/benefits. If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!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 $62,000.00 - $129,100.00. 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.

We are seeking Manager for our Laboratory Automation & AI Transformation Lab to join IQVIA Laboratories at Durham, NC.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Job Summary:Lead the transformation of our ligand binding bioanalytical laboratory into an end-to-end digitally orchestrated and physically automated operation powered by AI-assisted workflows. This role drives the design, deployment, and adoption of new ways of working across sample handling, instrument integration, digital data capture, automated review and reporting, and compliant documentation. What You'll Be Doing:Lead the automation transformation roadmap from concept through scaled deploymentDesign and optimize end-to-end workflows across sample receipt, preparation, analysis, data capture, review, and reportingManage change across scientists, Quality Control, and operations by addressing skill gaps, role evolution, and adoption needsLead a multidisciplinary team of automation engineers, scientists, and QC documentation specialists to deliver measurable resultsDefine and prioritize the automation product backlog, including requirements, delivery sequencing, and user adoptionEstablish effective operating rhythms such as sprint planning, standups, retrospectives, and release reviews where appropriatePartner with Quality to implement quality-by-design, validation strategies, change control, and inspection readinessDrive adoption through training, playbooks, ownership models, and clear exception-handling processes What We Are Looking For:Bachelor’s Degree in Science/Engineering or related field required5+ years in laboratory operations, lab transformation, automation programs, or digital lab systems.Experience implementing lab automation and/or digital lab platforms, including LIMS, ELN, and instrument integrationFamiliarity with validation approaches and regulated laboratory environments, including risk-based validation, CSV, 21 CFR Part 11 concepts, data integrity, and audit trailsOther equivalent combination of education, training, and experience may be accepted in lieu of degree The Knowledge, Skills and Abilities Needed for This Role:Strong leadership capability with experience guiding cross-functional technical teams through complex transformation initiativesExcellent communication and stakeholder influence skills across scientists, engineers, Quality, IT, and leadershipAbility to lead change effectively, resolve resistance through engagement, and build adoption into solutions from day oneLean and agile operational leadership in technical or regulated environmentsFamiliarity with AI-assisted workflows such as automated review, anomaly detection, and report drafting What We Offer You:We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.To learn more about our benefits, visit https://jobs.iqvia.com/benefits.If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!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 $80,200.00 - $167,200.00. 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.

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. We are seeking a US-based Senior Project Manager with proven experience in Oncology clinical trials to join IQVIA Biotech. This role is ideal for a seasoned project management professional who thrives in a fast-paced environment and is passionate about advancing therapies in the Immuno-Oncology space. You will leverage your expertise to lead complex, multi-regional studies and ensure operational excellence while building strong client relationships. OverviewAs a Senior Project Manager at IQVIA Biotech, you’ll play a critical role in accelerating the delivery of clinical trials and improving patient lives by bringing new therapies to market faster. You will lead core project teams, ensuring successful execution of clinical studies in alignment with contractual requirements, SOPs, and regulatory standards. This role combines strategic leadership, operational excellence, and customer engagement to deliver high-quality results. Key Responsibilities Lead bid defense presentations and contribute to study strategy development. Develop and implement integrated study management plans. Oversee planning and execution of medium to large, multi-regional clinical studies, ensuring speed, quality, and cost optimization. Serve as the primary point of contact for clients, fostering strong relationships and customer satisfaction. Build and lead cross-functional teams, driving collaboration and milestone achievement. Monitor project progress, manage risks, and resolve issues proactively. Ensure compliance with ICH GCP, local regulations, and company processes. Manage project financials, including forecasting, scope changes, and revenue acceleration opportunities. Mentor and support team members, promoting continuous improvement and knowledge sharing. Qualifications Bachelor’s degree in Life Sciences or related field. 7+ years of clinical research experience, including 4+ years in project management. Strong knowledge of clinical trial conduct, regulatory requirements, and therapeutic areas. Excellent leadership, communication, and negotiation skills. Proven ability to manage complex projects across geographies and functions. Proficiency in MS Office and project management tools. 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 $93,100.00 - $232,800.00. 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.

Job Overview IQVIA is hiring a clinical project manager to expand our dedicated Real World Evidence (RWE) FSP team, working fully within the environment of a prominent pharma company. In this role, the clinical project manager will be responsible for end-to-end project delivery of real-world observational studies within the oncology therapeutic area. It is important for this individual to have experience working in observational research across primary and secondary data collection study designs as well as leading clinical studies independently. Who do you work with? Epidemiologists, data science, and clinical leads to deliver project specific goals and timelinesVendors to communicate status of deliverables and workflowProgram and business leads to manage full portfolio of projectsWhat are you great at? Independently executing observational and real-world studies while balancing speed, quality, and costLeading cross-functional teams to achieve milestones and resolve study issuesProactively identifying risks and implementing mitigation plansCommunicating clearly with stakeholders, including preparing and presenting project updates to leadershipGood understanding of project financials including experience managing, contractual obligations and implicationsDriving operational excellence and strategic partnership with clientsManaging vendors effectively across different sourcing models (in-house, hybrid, outsourced)Bringing clarity to complex or ambiguous situations and making informed decisionsResults-oriented approach to work towards delivery and outputStrong organizational, prioritization, and time management skillsAbility to operate effectively in a matrixed, fast-paced, and evolving environmentYour responsibilities may include:  Leading global, cross-functional observational study teams and owning delivery of contracted scope, timelines, and qualityDeveloping study documentation, including project management plansEnsuring consistent use of study tools, training materials, and compliance with SOPs, policies, and proceduresMonitoring study progress and financial performance; supporting forecasting and change control as neededLead project vendor management related activities and communications per project requirementsAnticipating operational and quality risks, responding to issues raised by the project team and planning/implementing appropriate corrective or preventative actionsGenerating project- or program-level metrics and reports for senior managementCapturing lessons learned and contributing to continuous improvement and best practicesRequired knowledge, skills, and abilities   Bachelor's degree in life sciences or related field  Minimum 4-6 years of experience in project management and/or clinical operations within pharma, CRO, or RWE environment (or equivalent combination of education, training, and experience)Demonstrated experience leading observational or real-world evidence studiesStrong understanding of RWE study designs and clinical research conduct and skill in applying applicable clinical research regulatory requirementsExperience with primary and secondary data study designs  Therapeutic area expertise desired (oncology)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 $93,100.00 - $232,800.00. 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.

Senior Director, Customer Delivery Unit (Oncology Portfolio Lead) We are seeking an exceptional Senior Director to lead end-to-end delivery across a large, complex global oncology portfolio. This is a highly visible leadership role with direct client engagement, offering the opportunity to influence strategy, execution and partnership success at scale. You will play a pivotal role in delivering innovative oncology therapies to patients worldwide by driving operational excellence, leading high-performing teams, and strengthening one of our most strategic global partnerships. What You’ll Do Portfolio Leadership & Delivery: Provide strategic oversight of a global oncology portfolio for a customer dedicated delivery unit, driving high-quality and cost-effective execution across multiple studies to accelerate patient access Cross-Functional Leadership: Lead integrated cross-functional teams across clinical, data, regulatory, and safety to ensure alignment, visibility and proactive risk management across the portfolio Client & Partnership Leadership: Serve as a senior executive partner to clients, building trusted relationships while leading escalations and critical discussions to drive effective decisions and outcomes Governance & Strategy: Represent Customer Delivery Unit in executive governance forums, influencing portfolio strategy, delivery models and long-term partnership success Operational Excellence: Drive standardization, innovation, and continuous improvement by embedding best practices and scalable processes to enhance delivery performance People Leadership: Lead and develop senior leaders, building high performing, engaged teams focused on accountability and growth Business Growth: Contribute to business development and strategic initiatives by providing operational insights that shape competitive, winning solutions   What We’re Looking For 15+ years of experience in clinical development or clinical operations with deep oncology expertise Proven success leading large, global clinical portfolios with full operational and financial accountability Strong background in study leadership or clinical program delivery, with the ability to translate strategy into execution Demonstrated ability to operate at the executive level with clients, influencing decisions in complex environments Track record of building and leading high-performing, global teams Experience working within strategic partnerships or alliances preferred Education: Bachelor’s degree required; advanced degree (PhD, MD, PharmD, or MBA) strongly preferred Leadership Profile Visible, energizing leader who inspires teams and drives engagementStrong collaborator who fosters alignment and accountability across functionsStrategic thinker with a results-oriented mindsetPassionate about innovation, continuous improvement, and patient impactIQVIA 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 $140,500.00 - $391,200.00. 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.

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. Senior Director, Real-World Data Sales, EMEA IQVIA’s Market Measurement solutions provide reliable estimates of pharmaceutical market activity by integrating multiple data sources to track product performance, market size, and competitive trends. These insights help organizations make informed commercial decisions and identify growth opportunities. Complementing this, IQVIA’s Real‑World Data (RWD) assets capture health information from routine clinical practice, including electronic health records, claims, registries, and patient‑reported outcomes. RWD provides a detailed view of how treatments perform in real‑life settings, enabling deeper insights into patient journeys, disease patterns, and therapeutic effectiveness. Together, Market Measurement and RWD offer a powerful, end‑to‑end understanding of both market dynamics and real‑world clinical impact, supporting evidence generation and strategic decision‑making across the product lifecycle. We are seeking an experienced and consultative Senior Director of RWD Sales to develop and expand new business opportunities across EMEA. Primary client stakeholders include Pricing, Market Access, Medical Affairs, HEOR, and Late Phase study teams. Responsibilities 1) Client engagement and business understanding Maintains and strengthens professional relationships across client organizations, with a particular focus on Real‑World Data stakeholders.Develops deep client knowledge, including business priorities, organizational culture, product portfolio, pipeline, and budget focus.Manages a systematic client‑feedback approach to continuously improve the client experience.Acts as the go‑to person to diffuse tensions or complaints arising from IQVIA engagements.2) Operations management Leads operational management and oversight of IQVIA’s RWD activities across local and international markets.Manages strategic and key account relationships individually or in coordination with Global and Regional Sales Teams.Identifies and responds to customer needs, defining opportunities for RWD and proposing tailored solutions.Collaborates with IQVIA’s RFX, Pricing & Contracts teams to support the full sales cycle.Works closely with the Market Measurement team to align and support broader commercial strategy.3) Shaping client perception of IQVIA Identifies opportunities to engage clients with relevant marketing and thought‑leadership materials.Manages the annual Strategic Management Review conference.Creates opportunities for peer‑to‑peer engagement by introducing relevant IQVIA experts aligned with client interests.4) Bringing innovation to clients Leverages deep client knowledge to identify strategic discussions and major opportunities for IQVIA.Actively contributes to the Sales and Account Management community by sharing ideas and success stories from other major accounts.Requirements  Extensive knowledge of Real-World Data10+ years of experience in Sales, Business Development, or similar roles within pharma, CRO, health, life sciences, or other regulated industriesStrong understanding of Medical, Health Economics, Pricing & Market Access principlesProven track record managing mid‑ and senior‑level client relationshipsStrong organizational, planning, and project‑management skillsExperience engaging with outsourcing, procurement, and mid‑management stakeholdersExcellent business and industry awareness with strong understanding of market trendsStrong analytical skills for interpreting customer business dataAbility to manage demanding timelines and influence internal and external stakeholdersAbility to provide weekly CRM updates on client activities, RFX, and contract statusAbility to work creatively in a fast‑paced environment with exceptional attention to detailAbility to work independently and collaborativelyProficiency in Microsoft PowerPoint, Word, and ExcelExcellent oral and written communication skillsAbility to build and maintain effective working relationships with colleagues and clientsWhy Join? Those who join us become part of a recognized global leader still willing to challenge the status quo to improve patient care. In IQVIA, you will have access to the most cutting-edge technology, the largest data sets, the best analytics tools and, in our opinion, some of the finest minds in the Healthcare industry. 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 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. It's 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 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.

Business Consultant (m/w/d) hybrid Dortmund / Vollzeit Health System Services (HSS) wurde 1990 gegründet und ist einer der führenden Technologieanbieter und Dienstleister im deutschen Gesundheitsmarkt. Zu den Schwerpunkten unserer Tätigkeit gehören das Genehmigungs- und Abrechnungsmanagement, die Softwareentwicklung und -bereitstellung sowie Digitalisierungs- und Archivierungsleistungen für Krankenkassen. Wir suchen dich für unseren Geschäftsbereich in Dortmund mit rund 170 Mitarbeitenden. Für unsere Kunden aus dem Bereich Banking & Finance entwickeln wir Software zur Digitalisierung von Geschäftsprozessen von der Architektur bis zur Implementierung. Dabei setzen wir auf Standard-Technologien, verlieren aber auch neue Entwicklungen nicht aus dem Auge. Du begeisterst Dich für Digitalisierung und smarte Prozesse und kannst deren Bedeutung für den Bankensektor sicher einordnen? Dann hast Du bei uns die Möglichkeit, künftig eine zentrale Rolle in unserem Service‑Management zu übernehmen. Als Teil eines Netzwerks aus erfahrenen Expertinnen und Experten arbeitest Du eng mit unseren Kunden zusammen und entwickelst innovative Konzepte zur Weiterentwicklung unserer Lösungen. Dabei begleitest Du die Einführung moderner Softwarelösungen und unterstützt die Umsetzung anspruchsvoller Projekte im gesamten Bankenbereich – von der ersten Idee bis zur erfolgreichen Umsetzung. Deine Aufgaben: Projekteinführung von Software bei Banken – inklusive fachlicher Vorbereitungen, Durchführung, Steuerung des Projektes und Unterstützung der Kunden während der Implementierungsphase Betreuung und Betrieb unserer Softwarekomponenten in den Produktivumgebungen unserer Kunden Selbstständige Analyse und Bearbeitung von Supportanfragen und Change Requests unterschiedlicher Dringlichkeit und Komplexität Fachliche Weiterentwicklung bestehender Softwareprodukte sowie Konzeption und Umsetzung neuer Features in enger Abstimmung mit Fachbereichen und Entwicklungsteams Mitarbeit in Projekten für den gesamten Bankenbereich, von der Anforderungsaufnahme bis zur Produktivsetzung Enge Zusammenarbeit mit den Bereichen Consulting, Entwicklung, Betrieb und Testmanagement Dein Profil: Abgeschlossene Ausbildung zum/zur Bankkaufmann/-frau oder eine vergleichbare Qualifikation Praktische Erfahrung im Bankenumfeld, idealerweise im Bereich der Marktfolge Interesse daran, bankfachliche Inhalte in Softwareprozesse zu überführen und fachliche Anforderungen verständlich aufzubereiten Bereitschaft, sich in technische Themen einzuarbeiten, um Konfigurationen, einfache technische Abläufe und produktbezogene Zusammenhänge sicher zu verstehen Bereitschaft zu gelegentlichen Dienstreisen Teamgeist, Flexibilität sowie lösungsorientierte Kommunikation Sicheres, serviceorientiertes Auftreten als kompetente/r Ansprechpartner/in – auch beim Kunden vor Ort Im Besitz eines Führerscheins der Klasse B Verhandlungssichere Deutschkenntnisse (mind. C1) in Wort und Schrift sowie gute Englischkenntnisse (mind. B1) Du profitierst unter anderem von diesen Benefits: Flexible Arbeitszeiten Möglichkeit von Homeoffice, inkl. entsprechender IT-Ausstattung 30 Tage Urlaub pro Jahr Kita Bezuschussung Betriebliche Altersvorsorge Kostenfreie Nutzung der LinkedIn Learning Plattform Strukturierte Einarbeitung, individuelle Weiterbildungsmöglichkeiten und regelmäßige Feedbackgespräche Dienstreisen zu Kunden, für deine Mobilität steht dir selbstverständlich ein Poolfahrzeug zur Verfügung Fitnessbereich und Lounge mit Kicker und Spielekonsole im Büro Team- und Unternehmensevents kostenlose Kalt- & Heißgetränke Wir schätzen Vielfalt und begrüßen daher alle Bewerbungen – unabhängig von Geschlecht, Nationalität, ethnischer und sozialer Herkunft, Religion/Weltanschauung, Behinderung, Alter sowie sexueller Identität. 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.

To be eligible for this position, you must reside in the same country where the job is located. Job Overview Secure and retain business through professional, consultative, proactive sales activities directed at decision-makers and decision influencers at existing and new clinical sponsors. Essential Functions Actively prospect and leverage potential new business opportunities within specified customer account(s). Cultivate strong, long-term relationships with key decision-makers within Account and develop in-depth knowledge of the customer organization. Maintain general knowledge of all IQVIA services for appropriate cross-sell opportunities. Aggressively pursue awareness of competitive activities, positioning and pricing, which includes specific reasons for awards and non-awards. Identify and respond to customer needs in order to define potential opportunities.  Propose appropriate strategy/solution to customer. Coordinate with contracts/proposals to develop proposal. Work with operations and functional managers to identify sales team and prepares and leads the sales presentation. Educate team participants in customer culture, operational needs/methods and sales techniques needed to close the sale. Handle follow-up related to the sale and drive completion of contractual documents. Adapt successful strategies and tactics to meet market demands and financial targets. Maintain high visibility within customer organization.  Monitor customer satisfaction by communicating regularly with customer. Establish and execute a comprehensive sales plan for each target account.  Ensure appropriate strategy/solution is proposed to customer.   Monitor actions and results against plans. Analyze potential opportunities and develop sales plans for each target account. Ensure appropriate strategy/solution is proposed to customer. Monitor actions and results against plans. Record all customer sales related activities in CRM system. Prepare sales activity report for Sales Management as required. Serve as a liaison between the customer and technical and operational groups at IQVIA, Inc. Qualifications Bachelor's Degree in Business Management Req 10 years related experience, including 3 years of relevant industry (CRO/Pharmaceutical) and/or sales experience Req Or Equivalent combination of education, training and experience Req Proven track record at mid-level and high-level contacts Strong organizational, planning, project management skills A developing record of customer contacts at the outsourcing, procurement and mid - management level Excellent Business/Industry awareness and a thorough understanding of industry trends and impact on the business Excellent analytical skills in assessing and interpreting customer business data Ability to maintain demanding timelines Ability to influence others internally and externally Adaptability and flexibility to changing priorities Demonstrated ability to work creatively in a fast-paced environment Exceptional attention to detail and ability to work simultaneously on multiple priorities Ability to work independently and as a team player Excellent skills using Microsoft Office Suite: MS PowerPoint, MS Word, and MS Excel Excellent oral and written communication skills Ability to establish and maintain effective working relationships with coworkers, managers and clients 30-40% travel is required (based on location). To be eligible for this position, you must reside in the same country where the job is located. 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 $89,600.00 - $249,600.00. 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.

Develop the regional contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor’s requirements. Essential Functions Coordinate the development of investigator grants and estimates, contracting strategies and proposal text to support the proposal development process.Develop contract language, payment language and budget templates as required as applicable to the position.Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan.Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements.Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and the wider company, as required.Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreements.Work with Quality Management to ensure appropriate contract management and quality standards. Mentor and coach colleagues as required including the delivery of training materials as required.Deliver presentations to clients as required. As applicable, eEnsure accurate completion and maintenance of internal systems (with emphasis on CTMS), databases, tracking tools, timelines and project plans.Qualifications Bachelor's Degree Related field Req.3 year relevant sponsor or clinical research organization clinical site contracting experience, including demonstrable global and/ore regional experience acting as a contract negotiator. Equivalent combination of education, training and experience.Good negotiating and communication skills with ability to challenge.Good interpersonal skills and a strong team player.Strong legal, financial and/or technical writing skills.Strong understanding of regulated clinical trial environment and knowledge of drug development process.Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.Knowledge of applicable regulatory requirements, SOPs and company’s Corporate Standards.Ability to exercise independent judgment, taking calculated risks when making decisions.Ability to lead, motivate, coach and mentor.Good organizational and planning skills.Good presentation skills.Good understanding of clinical trial contract management. 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 Review, assess, and process safety data and information across service lines, received from various sources. Distribute reports/data to both internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs), and internal guidelines under the guidance and support of senior operation team members. This is a trilingual role requiring fluency in English, Spanish, and Italian. Main Responsibilities Process safety data according to applicable regulations, guidelines, SOPs, and project requirements.Perform pharmacovigilance activities, including collecting and tracking incoming Adverse Events (AEs) and endpoint information, determining initial/update status of incoming events, database entry, coding AEs and products, writing narratives, and literature-related activities.Ensure compliance with quality, productivity, and delivery standards per project requirements.Liaise with different functional team members and healthcare professionals to address project-related issues. Qualifications Bachelor’s degree in Life sciences or a related field (mandatory)Fluency in English and Italian (mandatory) (will be evaluated)Up to 3 years of previous clinical experience (desirable)1 year of pharmacovigilance experience will be highly valued (desirable) What we offer to you: OSDE 310Annual bonus by performanceSalary adjustments during the year according to inflation rates.21 vacations daysWork flexibility100% remote role!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 OverviewManage the financial consolidation process, including the recording of topside journal entries, the preparation of the financial statements including roll-forwards and the preparation of internal financial reports including analysis to show variances between actual and forecast budgets. Essential Functions• Undertake financial analysis of key data for assigned issues and areas using a variety of reporting tools to compare actual performance with forecasts and budgets and provide management with information of trends and results to enable corrective action to be taken.• Responsible for booking month-end entries to produce the final trial balance for respective month.• Record recurring topside journal entries and act as the contact person for recording topside entries required by the operating units.• Book various tax entries and run reports for the tax department.• Prepare and maintain the consolidating income statement and balance sheet for use by external reporting and for review by the independent auditors.• Prepare a roll-forward of changes since the previous version provided to management and the independent auditors to illustrate changes to the income statement, balance sheet and cash flow.• Prepare the consolidated flux analysis; a key management control and a vital source of analysis for the independent auditors.• Coordinate all the responses from the operating units to explain the variances or changes outside the agreed tolerances. Follow up with the units if the explanations provided need further elaboration.• Maintain a detailed understanding of internal customer requirements and develop processes that will meet or exceed these requirements. Provide analysis of key data and identification of trends to support and advise managers.• Ensure compliance with internal financial accounting procedures and policies relevant to the scope of this role.• Perform other duties as assigned. Qualifications• Bachelor's Degree  Req• 7 years’ experience in accounting Req Or• Equivalent combination of education, training and experience. Req• Comprehensive technical accounting skills.• Knowledge of finance modules of Enterprise Resource Planning (ERP) systems such as SAP, PeopleSoft.• Knowledge of Microsoft Office applications.• Strong analytical and numeracy skills.• Ability to identify financial issues, develop and execute mitigating actions.• Effective verbal and written communication skills.• Strong influencing skills.• Ability to prioritize and coordinate multiple work requirements to meet deadlines.• Ability to establish and maintain effective working relationships with co-workers, 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.

Collaborate with pre and post award stakeholders to manage the coordination, planning, quality and implementation of Patient Recruitment and Retention operational plans on small/mid size studies. Position may be responsible for the implementation of smaller programs in their entirety. Communicate with sponsors and project teams to implement and monitor impact of the recruitment/retention tactical plan; make additional operational and tactical recommendations as needed based on study performance.  Collaborate with internal teams and external providers to deliver all appropriate tactics associated with the recruitment/retention strategy. Represent IQVIA Patient Recruitment at site/sponsor-facing meetings (i.e. KOM, IM, F2F/LL, etc.) to present strategy/rationale, train CRAs and site staff, and conduct recruitment support workshops as required. Ownership for study KPI and financial performance. Essential Functions• Work together with strategy team to translate recruitment and retention strategy into operational and tactical plans to positively impact recruitment and retention rates for assigned projects• Serve as internal consultant to project teams to implement operational recruitment plans on new and/or existing projects needing recruitment and retention services• Manage the scope of work, objectives, quality of deliverables, and other activities of assigned projects (based on scope, may co-manage or independently manage these projects)• Serve as primary operational project contact for patient recruitment and retention programs with sponsor to ensure appropriate communication channels are maintained and reporting schedules adhered to as required• Management of assigned project budget(s) to meet financial and company goals (realization targets)• Coordinate operational and tactical related project activities for study team and sponsor to ensure that overall project milestones are met• Develop and implement risk management plans for minimizing impact on project objectives and deliverables• Other duties as assigned by Management• Maintain knowledge of current recruitment trends, vendors, and technologies to increase productivity and recommend additional support as needed• Leverage internal intelligence to support and refine strategy on assigned projects• Provide technical expertise as able in support of project specific and interdepartmental training efforts• Support continued process improvement to ensure quality in the department Qualifications• Bachelor's Degree Health care or other scientific discipline• Over 3 years of relevant industry experience, with +1 years of experience in a project management role, is mandatory.• In depth knowledge of the drug development processes across all functional areas • Good written and verbal communication skills including good command of English (this will be tested)• Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines• Excellent organizational and problem solving skills• Effective time management skills and ability to manage competing priorities• Strong interpersonal skills effective presentation skills• Ability to establish and maintain effective working relationships with coworkers, managers and clients• Computer skills including proficiency in aspects of data analysis and presentation software, Microsoft Word, and Excel 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.

Core Responsibilities: • Month end close, blackline• Compliance control• Order and contract maintenance (changes to prices, users, data period etc.)• Billing• Revenue recognition• Process accruals and other templates such as revenue/product/client transfers• Upload information to Blackline• Preparation of required docs for month end close for local finance teams• Attendance of internal training sessions• Organization of monthly calls with local office• Maintain country specific documentation needed for processing and keep them updated• Preparation of samples for SOX audits  Required skills/Characteristics:• Commercial studies/school or commercial apprenticeship• 1-year experience in finance, administrative, or customer support• Tool knowledge – SAP, PeopleSoft Finance, Oracle – nice to have• Fluent in English (oral and written) is a MUST• Fluent knowledge of German OR French OR Italian OR Spanish is an asset• Good team player• Service and client oriented• Open to take over new work and can easily adapt to changes• Positive, friendly and flexible• Punctual and accountable• Efficiency oriented• Solution focused 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.

Internal Job DescriptionJob Title: Account AssistantLocation: Bournemouth, UK (Please note, this is a HQ based role - 5 days/week; with flexibility to work remotely 1 day/week post probation/assessment)Grade: 120 Are you looking to develop your finance career in a dynamic, collaborative and growing organisation? We are seeking a proactive and detail-focused Accounts Assistant who enjoys working with numbers, improving processes and supporting colleagues across the business. This role is ideal for someone with experience in expenses, reconciliations and accounting systems who wants to broaden their finance expertise and work within a forward‑thinking team.About the RoleAs a Accounts Assistant, you will support the smooth running of core transaction processing activities. You will handle expenses, reconciliations, invoice processing and BACS payment preparation while maintaining strong internal controls and high levels of accuracy. You will also support integration projects and work alongside the Transaction Processing team to deliver consistent, efficient and well‑documented finance processes.This position offers a great opportunity to deepen your SAP knowledge, build technical capability and develop within a supportive finance function.Key ResponsibilitiesExpense and Credit Card ProcessingReview expense and credit card claims for completeness, accurate VAT treatment, correct account coding and compliance with Group policy.Prepare the expense payment file for approval, generate the approved BACS file and set up payments for final release.Reconcile all outgoing payments with ledgers and the credit card system.Invoice and PO SupportProcess invoices into live systems in a timely and accurate manner.Support colleagues across the business with purchase order creation and enquiries.Process Alignment and IntegrationWork with integration teams to align and roll out new processes.Support the Transaction Processing Manager, Team Leader and transformation specialists in developing standardized transaction processing procedures across the Group.Internal Control and ConfidentialityUphold strong internal controls and maintain confidentiality in accordance with data protection regulations.Team CollaborationContribute to the Transaction Processing team, providing support and holiday cover for colleagues and receiving the same in return.Carry out any other reasonable tasks aligned to the role.Skills & Qualifications1-2 years experience in an accounting or expenses role, including reconciliations and double entry journal posting.Experience delivering strong customer service to employees, suppliers and stakeholders.Confident using computerized accounting systems, ideally SAP.Experience with both automated and manual reconciliations.Part‑qualified AAT or equivalent finance qualification is desirable.Good general education including strong literacy and numeracy skills.Intermediate Excel skills, including the ability to extract, manipulate and reconcile data.Strong organisational skills and attention to detail.Ability to work to deadlines while maintaining accuracy and quality.Adaptable, proactive and comfortable working in a fast‑moving environment.Committed to maintaining confidentiality and protecting employee and client data.Why Join Us?- Be part of a dynamic team where support, collaboration, development and continuous growth is encouraged.- Work and learn from the Finance experts.- Strengthen your accounting knowledge, gain exposure to integration projects and build a strong platform for progression within finance.If you are motivated, curious and ready to take the next step in your finance career, we would be delighted to hear from you.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.

Role: Delivery and People Lead, HQ Advisory, CSEC Commercial Solutions Excellence Centers (CSEC) Mission CSEC is a global function that will centralize global delivery across key commercial offerings and will be the engine powering the future of our global Commercial Solutions. By centralizing global and regional teams, we are unlocking scale to deliver quality, efficiency, and innovation—shaping the next generation of solutions for our customers. Our mission is clear: to combine diverse talent with automation and AI to accelerate commercial excellence worldwide. We will actively partner with regional business unit leadership teams to foster strong collaboration, optimize the delivery model by combining local and global centers, and improve delivery performance. Job Overview This role leads Advisory delivery teams internationally within CSEC, managing Workday processes, staff, team culture, social events, and performance development. As Delivery leader on multiple projects, ensure strong client satisfaction, project outcomes, and effective teamwork in collaboration with DTAS senior staff. The position upholds quality standards, provides coaching, coordinates training, and requires deep expertise in at least one consulting area (Commercial Strategy & Transformation, Asset & Portfolio Strategy, Value and Access, Medical Strategy, AI & Advanced Analytics, Integrated Digital Health) for enhanced project results and clear client communication. Key Responsibilities Office and People Management Line manager to the CSEC HQ Advisory team within one or more offices. Current offices are in Europe, United States, Mexico and India.Manages office communication (within team and to senior leadership) and team engagement through internal meeting co-ordination (e.g. monthly town halls)Responsible for HR and Workday activities linked to line management responsibilities including recruitment, managing individuals’ performance in collaboration with the individuals DL (Development Leader), and take talent management actions in collaboration with HR, and all related Workday processesActively mentors and coaches the teamLeads individual discussions on performance, compensation, bonus and career options.Works with global and regional Advisory leadership to manage local headcount, grade distribution, and attrition for effective headcount planning.Responsible for team performance management, including annual reviews in collaboration with Advisory leadership and Development Leads (DLs).Mentors, coaches, and shares subject matter expertise with the team to help develop individuals and capabilities that support career development.Supports the implementation of new innovative tools / AI tools to drive increased productivity, efficiencies or quality in delivery, including facilitating the piloting of tools within projects and providing feedback to developers.Foster a positive culture of accountability, collaboration, inclusion, and continuous learning, with regular attendance in the office.Project Delivery Leads multiple projects, in collaboration with DTAS Advisory seniors.Ensures client materials, reports, and presentations are consistently high quality and insightful, delivering all or significant portions of findings to client while balancing resource considerations.Balances revenue and resource considerations to achieve commercial objectives for CSEC, while supporting DTAS goals such as profitability and competitiveness.Ensures team utilization aligns with budget and timelines, proactively escalating risks to DTAS and driving solutions such as scope extensions where required.Prioritizes tasks and objectives effectively, managing time and resources appropriately, setting realistic deadlines, and preparing contingency plans.Identifies innovative ways to delivery projects with increased quality, efficiencies or productivity.Maintains accountability for client satisfaction and the delivery of high-quality, value-added outcomes in collaboration with DTAS team.Demonstrates high level of expertise in key consulting areas and project types, such as in Commercial Strategy & Transformation, Asset & Portfolio Strategy, Value and Access, Medical Strategy, AI & Advanced Analytics, Integrated Digital Health.Provides on-project coaching / leadership within given area of expertise to delivery teams.Collaborates with DTAS senior stakeholders to define future skill sets required for CSEC Advisory teams.Competencies Empathetic team leader who upholds our team’s culture and values in the team.Balances team vs. business priorities effectively and with consideration.Communicates clearly and adapts to audience and situation.Collaborative and solution-oriented way of working across the business.Adapts quickly to change and shifting priorities.Proactive, acts with initiative and accountability.Uses analytical skills to solve problems and handle complexity.Comfortable with technology and helps others adopt innovative solutions.Qualifications Bachelor's Degree required, Master's Degree preferred.At least 7-8 years professional experience in consulting, pharmaceutical and healthcare industry with evidence of career progression.Demonstrable experience in and commitment to the life sciences and/or healthcare industries.Proven experience in managing a team and identifying, recruiting, mentoring/coaching, and retaining top talent.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 $140,200.00 - $390,600.00. 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.