IQVIA

IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen. Werden Sie Teil unserer Community von rund 86.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welche Rolle Sie bei IQVIA einsteigen, es erwartet Sie ein offenes, innovationsfreudiges Umfeld, in dem Sie sich viel bewegen können. Finden Sie heraus, wie Sie Ihre Talente und Ihre Leidenschaften bei IQVIA einbringen können. Im Bereich Commercial Engagement Services (CES) arbeiten wir eng mit unseren Life Sciences-Kunden zusammen und unterstützen sie mit flexiblen Vertriebs- und Personallösungen für nachhaltigen Erfolg am Markt. Dies umfasst insbesondere die Rekrutierung, das Training und die Steuerung des Vertriebsteams in Dienstleistungsprojekten bzw. in Arbeitnehmerüberlassung. Dabei differenzieren wir uns über integrierte Projektansätze entlang des IQVIA Lösungsportfolios, die wir individuell an die Kundenbedürfnisse anpassen und aus einer Hand anbieten. Für unseren Kooperationspartner suchen wir einen Pharmaberater (m/w/d) für den Bereich Kontrastmittel als Vertriebs- und Applikationsspezialisten zum nächstmöglichen Zeitpunkt in der Direktvermittlung Im Gebiet: Nordostdeutschland Das sind Deine Aufgaben: Durch die intensive Betreuung ausgewählter Ärzte förderst Du den Verkauf von Kontrastmittel und Medizintechnik an Fachärzte und Kliniken und trägst so maßgeblich zum Unternehmenserfolg bei. Du setzt als Experte auf der Basis Deines Fachwissens Beratungsstrategien erfolgreich um und überzeugst so Deine Ansprechpartner.  Du findest mit Deinen Gesprächspartnern innovative Therapiekonzepte in anspruchsvollen Indikationen. (optional: zum Wohle des Patienten/für den Patienten/und trägst somit zur Gesundheit und dem Patientenwohl bei) Du führst regionale und zentrale Fortbildungsveranstaltungen in enger Abstimmung mit dem Regionalleiter und Deinem regionalen Team durch. Das bringst Du mit: Du hast die notwendige Qualifikation zum/zur Pharmareferenten/in oder Pharmaberater/in nach §75 AMG Du bringst Berufserfahrung im relevanten Umfeld, z.B. im Vertrieb von Medizinprodukten und/oder medizinischen Präparaten mit Klinikaußendiensterfahrung und/oder Key Account Erfahrungen sind wünschenswert Know-how Betreuung und Entwicklung von absatzfördernden Maßnahmen Erfahrungen und Fertigkeiten im Zusammenhang mit Projekt- und Teamarbeit  Erfahrungen im Umgang mit Großkunden/Gesundheitspolitik Betriebswirtschaftliche/kaufmännische Kenntnisse Hoher Grad an Selbstorganisation, hohe Eigenmotivation und Sozialkompetenz Gute kommunikative Fähigkeiten  Sehr gute Deutschkenntnisse, sowie gute Englischkenntnisse Das erwartet Dich bei uns: Ein attraktives Gehaltspaket plus Kundenprämien, vielfältige Corporate Benefits, betriebliche Altersvorsorge sowie 24/7 Unfallversicherung (auch für den privaten Bereich) und exklusive private Krankenzusatzversicherungen Ein top ausgestatteter Firmenwagen verschiedener Premiumanbieter mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des Modells  Eine moderne IT-Ausstattung für Deinen modernen digitalen Arbeitsplatz Unser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige Perspektive Wir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines Wohnorts  Eine hohe Übernahmequote durch unsere Kunden ermöglicht Dir den Karrierestart bei zukunftsweisenden und führenden Unternehmen der Pharmabranche und Medizintechnik-Branche Vielfältige und individuelle Weiterentwicklungsmöglichkeiten auch innerhalb von IQVIA (z.B. Führung, Key Account Management, Projektmanagement und vieles mehr) Wir begleiten Dich während Deiner Bewerbungsphase durch individuelle Betreuung/Vorbereitung bis zur Einstellung und auch darüber hinaus während des Beschäftigungsverhältnisses Unser Kunden-Netzwerk reicht vom Start-up Unternehmen bis zum Global Player. Gemeinsam mit Dir finden wir den richtigen Job für Dich! Starte Deine Karriere mit IQVIA! Dein besonders schneller Draht zu uns: Kandidaten-Hotline: 0621-84508113 oder sende uns gerne direkt Deine Bewerbung per Mail an: [email protected]  #LI-CES #LI-DNP #LI-SS2 #Pharmaberater #Medizinprodukteberater #Biologie #Chemie #Pharmareferent #BTA #CTA #PTA #Oecotrophologie #Pharmazie #Pharma-Außendienst #applynow #iqvia #weareiqvia 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 Opportunity IQVIA is currently recruiting for an Associate Consultant within the Primary Intelligence team. The successful candidate will have the opportunity to work with experienced healthcare consultants on integrated research solutioning to deliver comprehensive market insights to our clients in the healthcare industries. Job Responsibilities Manage both online and offline desk research to support proposal design and final reporting Perform Analysis of both qualitative & quantitative data to assist in the identification of client issues and the development of client deliverables Responsible for quality control of qualitative and quantitative data research Perform QC call back to the research respondents where necessary Assist consultants in day to day project operations where applicable i.e. preparation of research materials, agreements, presentation slides and other documents for research fieldwork Develops broad knowledge of related research methodologies and pharmaceutical market through the delivery of client engagements Creates presentations for clients with some senior support Attends, supports, and presents at client meetings with senior support. Contributes to learning, development and recruiting Desired Skills and Experience: At least 3 - 5 years of market research experience (preferably Pharmaceutical and Consumer Health market research) A good network with interview subjects (e.g.: Physicians, Pharmacists, and MOH officers) will be additional advantage Resourceful in contracting fieldwork agencies/freelancers to manage the load of fieldwork Strong proficiency in MS Office and written and spoken English is a must Ability to think creatively, and develop innovative solutions to uncommon problems - Intellectual stimulation makes consulting fun, and we hire people who bring a different point-of-view to the table Previous experience within healthcare industry in both qualitative and quantitative project management skill will be advantageous 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.

Clinical Trial Psych Rater - Spanish SpeakingLocation: Remote/VirtualHours: Estimated 10–16 hours per monthRole: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials. Position Overview The Clinical Specialist plays a key role in ensuring the integrity and reliability of clinical trial data. This position involves reviewing scales administered by raters to confirm standardized assessment practices. Responsibilities include evaluating assessment quality, engaging in live discussions with raters to provide guidance on methodology and scoring techniques, and supporting rater performance through functional assessments (e.g., mock interviews). Additional tasks may include assisting with communication materials and documentation. Key Responsibilities Participate in all required orientation, training, and calibration activities. Review case data and prepare for rater discussions, ensuring all relevant documents and scale items are available. Conduct live interactions with raters to provide feedback and guidance on assessment methodology and scoring. Complete assigned tasks and rater interactions according to schedule. Submit all required documentation accurately and on time. Required Qualifications Education: Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent). MD, DO, or PhD preferred. Experience: Minimum 3 years administering psychiatric assessments, rating scales, and/or structured clinical interviews (specifically EQ-5D-5L (Interviewer administered and Proxy 1 version) & mRS). Minimum 3 years of clinical experience with psychiatric populations. Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral research). Experience in CNS trials preferred. Skills: Strong interpersonal and communication skills for professional interaction at all levels. Excellent organizational skills, attention to detail, time management, and problem-solving ability. Proficiency with Windows and Microsoft Office applications. Language Requirement Current openings require fluency in English and native-level proficiency in Spanish. #LI-DNP #LI-Remote #LI-HCPN 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.

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, Commercial Sales & Operations, Brand Outsourcing & HCP Engagement IQVIA supports life sciences organizations with end-to-end solutions through deep industry expertise, advanced data and analytics, omnichannel engagement capabilities, and world-class talent. Our solutions enable clients to: Rapidly scale medical and commercial capabilities across geographiesDeploy flexible and efficient field engagement modelsAccess specialized resources and expertiseDrive operational excellence and commercial impactResponsibilities Commercial Leadership & Client Management Lead Commercial Sales Operations across a portfolio of international client accounts, ensuring effective and consistent delivery through International Project Directors and their teams.Serve as a senior point of contact for clients through governance meetings, performance reviews, business discussions, and escalation management.Build and maintain strong senior-level client relationships, positioning IQVIA as a strategic partner.Identify and pursue growth opportunities within existing accounts in partnership with Business Development, Global Account Directors, Finance, and delivery teams.Ensure project teams translate client strategies into actionable operational plans, clear deliverables, and measurable sales and activity KPIs.Operational Excellence Provide clear leadership, direction, and performance expectations for International Project Directors, International Project Managers, field leaders, and supporting operational teams.Ensure delivery of projects in accordance with sales targets, operational milestones, financial commitments, quality standards, and compliance requirements.Establish and maintain governance frameworks to monitor portfolio performance, risk management, financial performance, and strategic alignment.Leverage performance data, CRM reporting, client feedback, and governance outputs to identify risks and drive continuous improvement.Ensure teams operate with strong commercial discipline, compliant ways of working, and appropriate legal and governance standards.People Leadership Act as a strong leader, coach, and mentor to International Project Directors and senior operational leaders, fostering accountability, capability building, and succession planning.Lead recruitment, onboarding, development, and retention of leadership and field teams.Manage staff and managers in accordance with organizational policies and applicable regulations.Provide ongoing performance management, development opportunities, and employee relations support.Cross-Functional Collaboration Partner closely with Commercial, Operations, Medical, Compliance, HR, Finance, Talent Acquisition, and Business Development teams to ensure seamless project execution.Oversee third-party vendors and external partners supporting promotional delivery, ensuring performance aligns with contractual requirements and quality expectations.Ensure all activities are conducted in compliance with applicable regulatory, legal, and company requirements.Qualifications & Experience Required Significant experience within the pharmaceutical, biotech, healthcare, or life sciences industry.Experience in a senior commercial leadership role such as General Manager, Business Unit Lead, Head of Sales, Commercial Director, or equivalent.Minimum of 12 years of commercial sales, operations, client services, or delivery experience, including at least 10 years in people leadership roles.Proven track record of leading international commercial sales operations and large-scale client delivery programs across multiple markets.Demonstrated experience managing senior client relationships, governance structures, strategic account plans, and growth initiatives.Proven accountability for commercial performance, including achievement of sales objectives, KPI delivery, revenue forecasting, budget management, and margin optimization.Experience leading geographically dispersed teams, including project managers, field leaders, and operational teams.Preferred Experience within a consulting, outsourcing, contract sales organization, or other professional services environment.Experience managing complex international client portfolios and multi-country delivery models.Why Join? You can drive your career at IQVIA and choose the path that best defines your development and success. With exposure across diverse geographies, capabilities, and vast therapeutic and information and technology areas, you can seek opportunities to change and grow without boundaries. We know that meaningful results require not only the right approach but also the 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. 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.

Haz que tu talento transforme la práctica médica🌟Si ya cuentas con experiencia como Delegado/a de Visita Médica y te motiva participar en un proyecto dinámico y retador, esta puede ser tu próxima oportunidad profesional.Un importante laboratorio busca incorporar un/a Delegado/a de Visita a Atención Primaria para la zona de Alicante dentro de un nuevo proyecto temporal. Tu misión será visitar centros de salud y realizar encuestas a profesionales médicos para analizar hábitos de prescripción.🎯Tu misión: Serás el/la responsable de tu territorio, creando relaciones de confianza con centros de salud y profesionales sanitarios, aportando valor científico y contribuyendo a la consecución de resultados sólidos y sostenibles.📌 ¿Cómo será tu día a día?-Gestión integral del territorio: planificación, ejecución y seguimiento de objetivos y KPIs-Visita a centros de salud y contacto directo con médicos de Atención Primaria-Realización de encuestas para analizar hábitos de prescripción-Construcción y mantenimiento de relaciones profesionales de confianza-Análisis del entorno y detección de oportunidades en tu zona-Colaboración con otros equipos para maximizar el impacto del proyecto🚀 ¿Te apetece formar parte de un proyecto diferente, con impacto directo en el entorno sanitario y en el que tu experiencia marque la diferencia? ¡Esta es tu oportunidad!Ventajas sociales o económicas- Todas las herramientas de trabajo incluidas: vehículo de empresa, teléfono móvil, etc.- Excelente ambiente de trabajo, abierto e inclusivo.- Formación continua.- Acceso a plan de retribución flexible.Tipo de contrato:Fijo-discontínuoNúmero de vacantes:1Remuneración anual:35.000 € brutos/año + 10.000 € bonus#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.

This position will put you at the forefront of Patient Safety. As a MI/PV agent (dual role) you will have daily direct contact with Health Care Professionals (HCPs) and patients (the very people we are working to help), this is a highly visible and important role within IQVIA and essential to our core goal of patient safety. You will perform key medical information call center services and process safety and product quality information to help optimize the safety profiles of products across various therapeutic areas. You will benefit from joining the largest safety department in the world and working within an industry-leading, best-practice environment. To ensure you contribute to the business and grow your career, you will also benefit from ongoing training and development from our in-house safety experts to plan and progress your career.  Medical Information Specialists Responsibilities include receiving and documenting incoming telephone calls, voicemails, chats, faxes or emails from investigative sites or other sources reporting Lifecycle Safety Data.Additional responsibilities include: MI mailbox triage Translation of content where necessary. Receiving and documenting incoming calls, voicemails, chats, faxes, and emails from external customers such as patients and/or healthcare providers and responding to their enquiries about products. Summarizing these reports based on information identified as vital to the project. Triage, identify and transfer out of scope inquiries to local point of contact, as provided by the client. Disseminate clear, accurate information to healthcare professionals and patients based on the approved call scripts and/or other approved resources related to the use of client products. Creating Adverse Event and Product Quality Complaint reports requiring concise data entry covering everything from patient symptoms, admission, and results – this may include medical terminology, writing narratives, generating case queries Clarify, confirm, and capture adverse event and product quality information. PV Specialist An adverse event intake processor is responsible for reviewing, assessing and processing Lifecycle Safety data and information, across all service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and internal guidelines under guidance and support of senior operation team members. Responsibilities may include, but are not limited to: PV mailbox triage Receiving and sorting email case information Translation of information Send and monitor translations at vendor Redaction of source document personal identifiable information and attachment to case Review and data entry of specified fields in Argus and APEX databases Track workload and status of case processing in APEX Perform quality control of cases Case follow-up Reconciliation of cases against regulatory listings, Safety Data Exchange Agreement (SDEA), mailbox, etc. as needed. REQUIRED KNOWLEDGE, SKILLS AND ABILITIES  Bachelor’s Degree in a Life Science is required. .  Excellent written and verbal skills in German (native/C2), and English (min.C1) Willingness and aptitude to learn new skills across our Lifecycle Safety service lines.  Excellent attention to detail and accuracy maintaining consistently high-quality standards.  Excellent organizational skills and time management skills.  Ability to establish and maintain effective working relationships with coworkers, managers and clients.  Ability to work effectively on multiple projects simultaneously, organize own workload and effectively manage competing priorities.  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.

Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.• Collaborate and liaise with study team members for project execution support as appropriate.• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.• If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Qualifications• Bachelor's Degree Scientific discipline or health care preferred. Req• Requires at least 2 years of on-site monitoring experience. Req• Equivalent combination of education, training and experience may be accepted in lieu of degree. Req• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.• i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.• Good therapeutic and protocol knowledge as provided in company training.• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).• Written and verbal communication skills including good command of English language.• Organizational and problem-solving skills.• Effective time and financial management skills.• 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. 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.

IQVIA™ is The Human Data Science Company™, combining data, technology, advanced analytics, and human expertise to help healthcare clients improve outcomes for patients. Our solutions support better decision-making across the healthcare ecosystem and drive meaningful progress in life sciences. Team Overview IQVIA’s Financial Institutions Consulting (FIC) team advises investors (inc private equity, venture capital, hedge funds) on biopharma and life sciences investments, including commercial due diligence, asset and target screening, portfolio company growth strategy and exit/divestment strategy. Successful candidates will have the opportunity to engage with clients on high-profile strategic investment decisions across a variety of transaction situations, business models and strategic issues. We operate in a multi-cultural, collaborative and fast-paced work environment, that is rich in development and growth. Role & Responsibilities As a Consultant within IQVIA’s FIC team, you will be responsible for delivering projects primarily in the areas of due diligence (buy- and sell-side), asset/portfolio/company valuation, asset screening and growth strategy Leverage consulting and/or transaction advisory experience, IQVIA information and expertise, and methodological know-how to deliver discrete workstreams / modules that address client / business questions.Solve strategic issues / diligence questions through a structured and evidence-driven approach, working both independently or in small teams as part of project workstreamsDrive development of high-quality deliverables on a day-to-day basis, leveraging primary and secondary research approaches, including deriving analytical and qualitative insights to support assessmentsServe as a core team member and workstream lead, including responsibility for presenting / communicating key project insights and recommendations to project management / leadership – ensuring engagement satisfaction and supporting long-term enhancement of client relationshipsContribute to overall FIC team capabilities, including (but not limited to) the development of intellectual property, marketing materials, training, recruitment and proposal developmentAbout You Candidates interested in joining IQVIA FIC as a Consultant should have: Minimum of 4-5 years professional experience in strategy consulting, M&A/BD&L roles or within a financial institution (e.g. private equity, venture capital).Experience advising clients on commercial issues in the biopharma / life sciences industry and/or financial investors, including exposure to projects related to transactions / investments (due diligence, valuation, asset identification, growth strategy, forecasting)Experience working in multi-disciplined teams, including prior workstream oversight responsibilitiesStrong quantitative / analytical and qualitative research skillsets, supported by a problem solving mentality, keen eye for detail and critical thinking. Ability to drive primary/secondary research and analysis to assess business performance and synthesise findings into client deliverablesWell-developed written and verbal communication skills including presentations and report writingKnowledge of key issues and current developments in the biopharma / life sciences industryEvidence of career progression in consulting and/or transaction advisory rolesIn addition to the skills and experience above, a Consultant should have: Bachelor’s degree or equivalent. MBA not required but a plusFluency in English (spoken and written)A willingness and ability to travel (where required)Right to live and work in the recruiting countryBenefits We work hard to prioritise the things that matter most to you. Visit our benefits page for information on everything from perks to well-being initiatives and career enhancement. #CONAJD #LI-KS2 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 Summary  The Senior Human Resources Director will serve as a strategic HR leader supporting global business units within Global Clinical Development (GCD), R&D Solutions. Based in Europe, this role partners closely with senior executives on the GCD leadership team based globally, to drive organizational effectiveness, talent strategy, culture, and change leadership.   Key Responsibilities  Serve as primary HR Business Partner to Global BU leadership team members advising on organization design, workforce planning, talent, and culture.  Align HR strategy with global business priorities in partnership with the GCD Global HR Lead.  Use HR analytics and workforce insights to support data driven decisions.  Collaborate with global HR COEs (Talent Acquisition, Total Rewards, Leadership & Talent Development, HR Ops) to deploy scalable HR solutions.  Drive leadership development, succession planning, and employee engagement.  Lead reorganizations, M&A integrations, and workforce transitions.  Ensure adherence to local labor legislation while aligning with global standards.  Support leaders through change with clear communication and people first execution.  Oversee implementation of HR policies, compliance programs, and audit readiness.  Ensure timely HR reporting and insights to senior management.  Contribute to HR budgeting and identify opportunities to streamline HR processes.  Operate as a trusted advisor with strong influencing capability in a global, matrixed organization.  Collaborate with HR peers across R&D Solutions to ensure alignment of priorities and execution.  Qualifications  Bachelor’s degree required; advanced degree preferred.  CIPD qualification (Level 5 or above) or equivalent HR certification.  10+ years of HR generalist/specialist experience supporting senior leadership in complex, matrixed global organizations.  Preferred background in life sciences, CRO, technology, or consulting environments.  Expertise in organization design, leadership development, talent management, and engagement.  Demonstrated success leading change initiatives (reorgs, integrations, scaling transitions).  Strong knowledge of European labor legislation and multi country HR environments.  Exceptional judgment, communication, and problem-solving skills.  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.

Clinical Trial Psych Rater - Polish SpeakingLocation: Remote/VirtualHours: Estimated 10–16 hours per monthRole: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials. Position Overview The Clinical Specialist plays a key role in ensuring the integrity and reliability of clinical trial data. This position involves reviewing scales administered by raters to confirm standardized assessment practices. Responsibilities include evaluating assessment quality, engaging in live discussions with raters to provide guidance on methodology and scoring techniques, and supporting rater performance through functional assessments (e.g., mock interviews). Additional tasks may include assisting with communication materials and documentation. Key Responsibilities Participate in all required orientation, training, and calibration activities. Review case data and prepare for rater discussions, ensuring all relevant documents and scale items are available. Conduct live interactions with raters to provide feedback and guidance on assessment methodology and scoring. Complete assigned tasks and rater interactions according to schedule. Submit all required documentation accurately and on time. Required Qualifications Education: Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent). MD, DO, or PhD preferred. Experience: Minimum 3 years administering psychiatric assessments, rating scales, and/or structured clinical interviews (specifically PANSS, CGI-S). Minimum 3 years of clinical experience with psychiatric populations. Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral research). Experience in CNS trials preferred. Skills: Strong interpersonal and communication skills for professional interaction at all levels. Excellent organizational skills, attention to detail, time management, and problem-solving ability. Proficiency with Windows and Microsoft Office applications. Language Requirement Current openings require fluency in English and native-level proficiency in Polish. #LI-DNP #LI-Remote #LI-HCPN 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 is 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 OverviewProvide advanced technical expertise to develop and maintain programs to meet internal and external clients’ needs.  Plan and lead the development of project-related solutions to the full scope of statistical programming tasks.  Provide technical expertise to the Statistical Programming department. Essential Functions• Perform and plan: (i) the programming, testing, and documentation of programs for use in creating statistical tables, figures and listing summaries, (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 the integration of databases from multiple studies or sources.• Develop programming documentation including plans and specifications, as appropriate.• Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to teams and department.• Perform and plan the development, implementation and validation of new process technologies, macros and applications.• Fulfill project responsibilities at the level of statistical team lead for single studies, under supervision.• Understand the Scope of Work, estimate the work completed, and manage Out of Scope for single studies. May manage budget and resource requirements and provide revenue and resource forecasts for single studies. May be required to understand budget and quote assumptions.• Provide training and guidance to lower level and new staff. Qualifications• Master's Degree Computer science or related field and 1 year relevant experience Req Or• Bachelor's Degree Computer science or related field and 2 years relevant experience Req• Equivalent combination of education, training and experience Req• Knowledge of statistics, programming and/or clinical drug development process• Working knowledge of computing applications such as Base SAS, SAS/STAT and SAS Macro Language• Good organizational, interpersonal, leadership and communication skills• Ability to effectively handle 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.

Nous sommes à la recherche d’un(e) Gestionnaire associé(e) des services de projets en laboratoire pour se joindre à l’équipe des laboratoires d’IQVIA dans un poste en télétravail au Canada. Nous embauchons des innovateurs passionnés qui font progresser les soins de santé grâce à une collaboration réfléchie et inclusive. Si vous souhaitez donner un sens plus profond à votre carrière, joignez-vous à nous alors que nous transformons et accélérons la recherche et le développement. En tant que Gestionnaire associé(e) des services de projets en laboratoire, vous serez responsable de la gestion de tous les aspects liés au laboratoire pour les projets d’essais cliniques assignés à un client ou à un programme spécifique. Vous serez le principal point de contact du client après l’attribution de l’étude et pendant tout le cycle de vie de l’étude (démarrage, maintien, clôture), tout en vous assurant que le travail est effectué conformément aux procédures opérationnelles normalisées, aux politiques et aux bonnes pratiques. Ce que vous ferez :Faciliter la mise en place fluide des études, incluant l’examen des protocoles et budgets, la direction des réunions, l’élaboration et la mise en œuvre des plans de projet, des jalons, des registres de risques, de problèmes et d’actions. Participer aux processus de soumission de propositions et de développement des affaires, y compris les réunions de défense de soumission. Assurer le suivi du plan de gestion de projet, des échéanciers, des livrables, et gérer la documentation de l’étude durant tout le cycle de vie du projet, y compris l’archivage dans le système eTMF. Gérer les changements de portée de l’étude et surveiller le budget, la qualité de l’étude ainsi que toute problématique liée aux services, en mettant en œuvre les ajustements nécessaires. Développer et entretenir la relation avec le client, faciliter la communication, et collaborer avec toutes les équipes opérationnelles de l’entreprise. Coordonner le suivi des sondages auprès des clients et les vérifications régulières de satisfaction pour renforcer la relation client. Représenter l’entreprise lors de réunions d’investigateurs et d’autres réunions internes/externes en personne. Établir des canaux de communication réguliers avec les sites pour gérer les attentes et les enjeux du projet de façon continue. Ce que nous recherchons :Diplôme de baccalauréat en sciences de la vie ou dans un domaine connexe (préféré). Minimum de 2 ans d’expérience dans l’industrie clinique ou de la recherche, dont au moins 1 an en gestion ou mise en place de projets (préféré). Une combinaison équivalente de formation, d’expérience et d’éducation pourrait être acceptée en l’absence de diplôme. Expérience démontrée dans la gestion réussie d’essais cliniques de phases I à IV (préféré). Connaissances, compétences et aptitudes requises :Connaissance des processus de gestion de projets, des processus en laboratoire de l’entreprise et/ou connaissance équivalente des opérations de laboratoire central (trousses/fournitures, logistique, opérations de laboratoire, entreposage des spécimens, rapports et transferts de données, alertes sites, etc.). Capacité à travailler dans un environnement rapide tout en démontrant de solides compétences organisationnelles et le respect des échéances. Maîtrise de Microsoft Office et des systèmes de l’entreprise, ou expérience équivalente avec des systèmes de laboratoire centralisés similaires. Capacité à établir et maintenir des relations de travail efficaces avec les collègues, gestionnaires et clients. Vous devrez travailler directement avec des départements, des équipes, des fonctions de support et des parties prenantes d'IQVIA situés partout au Canada et à travers le monde, par conséquent, une connaissance fonctionnelle de l'anglais, tant à l'écrit qu'à l'oral, est nécessaire à l'exercice des fonctions de ce poste. Ce que nous vous offrons :Nous plaçons nos employés au cœur de tout ce que nous faisons et nous nous engageons à leur offrir, ainsi qu’à leurs familles, des avantages qui répondent à leurs besoins variés et évolutifs. Nous investissons dans des programmes et des ressources de bien-être intégrés pour prendre soin de leur santé physique, mentale, émotionnelle, financière et sociale, afin qu’ils puissent s’épanouir tant à la maison qu’au travail, à chaque étape de leur parcours de bien-être. Pour en savoir plus sur nos avantages, visitez :👉 https://jobs.iqvia.com/benefits Si vous souhaitez réaliser votre plein potentiel, joignez-vous à l’équipe des laboratoires d’IQVIA pour rendre l’extraordinaire possible ! ------------------------------------------------------------------------------------------ We are seeking an Associate Laboratory Project Services Manager to join IQVIA Laboratories business in a remote position. 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. As an Associate Laboratory Project Services Manager, you will be managing all laboratory aspects of assigned clinical trial projects for a customer or a specific program for a customer. You will act as the main point of contact for the customer after study award and throughout the entire study lifecycle (startup, maintenance, closeout), while ensuring work is conducted in line with standard operating procedures, policies, and good practices. What you’ll be doing: Facilitating seamless study set-up including protocol and budget review, leading meetings, develop and implement project plans, milestone, risk, issue, and action logs. Participating in the proposal and business development process including bid defense meetings. Monitoring the Project Management Plan, timelines, deliverables, and manage study documentation throughout the project lifecycle including filing into eTMF. Managing study scope changes and budget monitoring quality of the study and any service-related issues, implementing changes as required. Building and owning the customer relationship, facilitating communication, collaborating with all operational areas within the company. Coordinating customer survey follow up and ongoing health checks to support customer relationship building. Representing the company at Investigator meetings and other internal/external face to face meetings. Establishing regular lines of communication with sites to manage on-going project expectations and issues. What We Are Looking For: Bachelor's Degree Life Sciences and/or related field preferred. 2+ years of clinical or research industry experience, including 1 year project management/project set up experience preferred. Or equivalent combination of education, training and experience may be accepted in lieu of degree. Experience in successfully leading Phase I-IV clinical trials preferred. The Knowledge, Skills and Abilities needed for this role: Working knowledge of Project Management processes, the company laboratory processes, and/or equivalent working knowledge of central laboratory operations (kits/supplies, logistics, laboratory operations, specimen storage, data reporting and transfers, site alerts, etc.). Working in a fast-paced environment while possessing strong organizational skills and a demonstrated ability to meet deadlines. Demonstrating computer proficiency with Microsoft Office and the company systems, or equivalent experience with similar centralized laboratory systems. Establishing and maintaining effective working relationships with coworkers, managers, and customers. You will be required to work directly with IQVIA departments, teams, support functions and stakeholders located across Canada and around the world therefore, a functional knowledge of English, both written and spoken, is necessary to perform the duties of this position. 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 business, to help make the extraordinary possible! 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 $76,700.00 - $102,249.72. 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 $76,700.00 - $102,249.72. 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.

Clinical Trial Psych Rater - Lithuanian SpeakingLocation: Remote/VirtualHours: Estimated 10–16 hours per monthRole: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials. Position Overview The Clinical Specialist plays a key role in ensuring the integrity and reliability of clinical trial data. This position involves reviewing scales administered by raters to confirm standardized assessment practices. Responsibilities include evaluating assessment quality, engaging in live discussions with raters to provide guidance on methodology and scoring techniques, and supporting rater performance through functional assessments (e.g., mock interviews). Additional tasks may include assisting with communication materials and documentation. Key Responsibilities Participate in all required orientation, training, and calibration activities. Review case data and prepare for rater discussions, ensuring all relevant documents and scale items are available. Conduct live interactions with raters to provide feedback and guidance on assessment methodology and scoring. Complete assigned tasks and rater interactions according to schedule. Submit all required documentation accurately and on time. Required Qualifications Education: Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent). MD, DO, or PhD preferred. Experience: Minimum 3 years administering psychiatric assessments, rating scales, and/or structured clinical interviews (specifically PANSS, CGI-S). Minimum 3 years of clinical experience with psychiatric populations. Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral research). Experience in CNS trials preferred. Skills: Strong interpersonal and communication skills for professional interaction at all levels. Excellent organizational skills, attention to detail, time management, and problem-solving ability. Proficiency with Windows and Microsoft Office applications. Language Requirement Current openings require fluency in English and native-level proficiency in Lithuanian. #LI-DNP #LI-Remote #LI-HCPN 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 is 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 OverviewUnder general supervision, manage and maintain database systems, including back-up, performance tuning, capacity planning, monitoring, and reporting critical events and documentation. This hands-on role requires strong technical expertise combined with effective communication and interpersonal skills. Essential Functions Provision MySQL/MariaDB, MSSQL instances, both in clustered and non-clustered configurations, and manage HA groups.   Configure and maintain database servers and processes, including monitoring of system health and performance, to ensure high levels of performance, availability, and security. Manage Production, QA, and development database environments.   Learn relevant business processes and understand the data flow, criticality, and dependencies.   Minimize database downtime and manage parameters to provide fast query responses.   Enroll users, maintain system security, and monitor user access to databases. Database version upgrades and security patching to comply with security.   Allocate system storage and plan storage requirements for database systems.   Refine and automate regular processes, track issues, and document changes.   Perform periodic health checks and reports on database systems.   Develop innovation, strategies, processes, and best practices. Configure and maintain Amazon Redshift clusters.   Troubleshoot and resolve database integrity issues, performance issues, blocking and deadlocking issues, replication issues, log issues, connectivity issues, and security issues. Qualifications Bachelor's degree or equivalent in Computer Science, Information Technology, or a related field Candidates with 1+ year relevant experience in Database Administration are preferred.  Good knowledge of database design, administration, and architecture   Knowledge of replication and cluster configuration in MySQL/MariaDB, MSSQL Knowledge of MSSQL high availability configuration and monitoring   Understanding of backups, restores, and recovery models   Strong knowledge of stored procedures and query optimization   Knowledge and understanding of all aspects of database tuning: software configuration, memory usage, data access, data manipulation, SQL, and physical storage   Ability to develop procedure documents and maintain detailed database-related documents   Good analytical, time management, troubleshooting, and decision-making skills Excellent written and verbal communication skills 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 Summary:The Shuttle Driver is responsible for providing safe and timely transportation services for Cedar Gate employees. This includes scheduled pick-up and drop-off, as well as supporting emergency transportation needs during the day. Key Responsibilities: Ensure early morning pick-up and timely drop-off of employees as per schedule Provide employee pick-up and drop-off support in case of emergencies during working hours Be available for night duty or extended hours when required Maintain vehicle safety, cleanliness, and compliance with company policies Qualificaitions Minimum 2 years of driving experience in related fields Active driver's licence Valley routes knowledge 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 OverviewWork as an integral member of investigator site staff managing the day-to-day coordination and execution of clinical studies in accordance with the protocol, contracted scope of work, good clinical practice, sponsor and standard operating procedures (SOPs) and any relevant local guidelines and regulations. Essential Functions• Provide clinical research support to investigators to prepare for and execute assigned research studies• Review study protocols, source document forms, other study-specific documents, and electronic data capture systems used to record clinical research data• Collect and submit regulatory/ethics documentation as required by the Federal Drug Administration (FDA) and other regulatory bodies governing the conduct of the study• Recruit and screen patients for clinical trials and maintain subject screening and enrollment logs• Orient research subjects to the study including the purpose of the study, procedures and protocol requirements such as timeline for visits• Maintain source documentation based on protocol requirements that adhere to Good Clinical Practice (GCP)/International Conference on Harmonization (ICH) documentation principles• Schedule and execute study visits and perform study procedures as delegated and supervised by the Principal Investigator• Handle lab testing and analysis including preparation of specimen collection tubes and lab logistics• Monitor subject safety and reports adverse events and reactions to Principal Investigator, study team members  and IRBs as appropriate• Correspond with research subjects to troubleshoot study-related questions or concerns• Participate in routine meetings with site study staff and Investigators to confirm study tasks are assigned and are executed to the expected standards• Actively involved in study data quality checking and query resolution• Perform a variety of complex clinical research procedures including but not limited to electrocardiogram (ECG), lab sample collection, spirometry, vital signs, dose verifications, cardiac telemetry monitoring, and questionnaire administration• Assist investigator in verifying that research study objectives are met on time, within budget and according to application protocol requirements, clinical research regulations and quality standards• Assist in providing training to new investigator site staff members on study-specific topics and requirements• Maintain adherence to investigator site staff training requirements by auditing and maintaining training records• Prepare for and as needed attends study monitoring visits, study audits and regulatory inspections with clinical research regulatory agencies• Adhere to standard operating procedures (SOPs) and other directives throughout the process• Assist research site with coverage planning related to staffing and scheduling for research projects Qualifications•  Degree in health care or other scientific discipline preferred• 3 years' experience as Site Clinical Research Coordinator as accepted in accordance with local country requirements. Equivalent combination of education, training and experience.• Sound knowledge of clinical trials.• Advanced knowledge of the principals of Good Clinical Practices (GCP).• In-depth knowledge of protocol and study-specific operating procedures, consent forms, and study schedules.• Sound knowledge of medical terminology.• Ability to prioritize, seek input, problem solve and work in a team environment.• Ability to maintain confidentiality.• Ability to establish and maintain effective working relationships with coworkers, managers and clients.•  Applicable certifications and licenses as required by country, state, and/or other regulatory bodies.•  Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) strongly preferred. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $62,800.00 - $157,100.00. 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.

The Primary Care Sales Representative is responsible for driving strong brand performance by effectively engaging targeted health care providers and key accounts within an assigned territory. This role executes against sales objectives, brand KPIs, and financial targets by delivering a compelling and differentiated value proposition while building trusted, long‑term customer relationships. Through disciplined pre‑call planning, effective objection handling, and thoughtful post‑call evaluation, the representative continuously improves performance and closes with clear, appropriate calls to action. Consistently achieve sales performance, brand KPIs, financial objectives, and marketing goals, meeting or exceeding all established targets.Develop and implement an effective call plan to meet call metrics, ensuring optimal coverage and frequency with key customers to maximize access and sales potential.Clearly articulate the client value proposition to assigned healthcare providers, and identify, engage, and maintain relationships with disease state experts and speakers/advocates to optimize brand performance.Continuously enhance understanding of customer needs, market landscape, competitors, segments, account dynamics, disease areas, product knowledge, clinical insights, and sales expertise; share relevant market intelligence with field teams, brand team, and sales management to foster alignment, anticipate market changes, and refine brand strategy and execution.Proactively address customer needs and expectations, manage challenges, cultivate trusted relationships, and facilitate mutually beneficial agreements between AbbVie and its customers.Prepare pre-call strategies using SMART objectives and conduct post-call evaluations to drive continuous improvement in sales performance.Effectively address objections, clarify misunderstandings, and respond to concerns, consistently achieving logical calls to action and closing every sales call.Qualifications Demonstrated history of success in sales within relevant therapeutic areas; prior experience in pharmaceutical industry roles such as physician/account-based selling, training, managed health care, specialty pharmacy, or marketing is preferred.Consistently upholds high standards and delivers exceptional performance.Generates impactful ideas for organizational growth and responds proactively to change.Provides innovative solutions to optimize business outcomes and resolve challenges.Takes ownership in problem-solving, considering broader organizational implications.Identifies customer styles and adapts selling approaches accordingly.Collaborates effectively within a matrix environment, fostering partnerships across district and matrix teams.Supports the team's efforts in identifying information resources and learning opportunities, both internal and external.Applies findings to inform and develop evidence-based sales strategies.Possesses strong business acumen, proficiency with business tools, and advanced strategic and critical thinking skills.Demonstrates comprehensive scientific, therapeutic, product, and competitive expertise and is recognized as an expert by stakeholders.Exhibits strong presentation skills.Proficient in English, both written and verbal (for non-English speaking countries).Job Requirements: Holds a bachelor's degree in biological sciences, pharmacy, business, or a related field, or has equivalent qualifications. Willingness to travel with some overnights Preferred Qualifications: 1+ years Primary Care/Immunology/Dermatology/Pharmaceutical Sales Experience 3+ years of business-to-business sales experience, military experience, healthcare sales experience #LI-CES IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is 100,000-120,000 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.

Shift: Monday - Friday, 8:30 AM - 5:00 PM Location: Irving, Texas Role and Responsibilities Label, receive, and process samples (blood, urine, tissue, stool, etc.) for clinical trials per specific protocol guidelines to include logging samples into and out of the department. Request and receive tissue samples from outside pathology facilities. Send tissue blocks to vendor to have slides cut and ship these slides to the study’s lab. Label, receive, and process samples (blood, urine, tissue etc.) for clinical trials per specific protocol guidelines to include logging samples into and out of the department. Record all data in specified forms per clinical trial (paper and electronic) with accuracy and responsibility. Enter data into departmental database. Recognize discrepancies in the data on the samples and coordinate with the clinical staff to correct. Organize and store all reagents according to safety instructions. Maintain equipment and a clean and orderly lab environment. Restock lab consumables at the end of the day. Manage inventory of clinical trial supplies and kits as well as departmental supplies. Administrative functions include filing, scanning, copying, and emailing of work documents. Ship or store samples as per protocol before the end of the shift. Prepare all collection tubes and aliquots for the next day’s clinic with accuracy and responsibility. Other duties as assigned. Minimum Qualifications and Education Requirements Lab Assistant training or associate degree in the Sciences or an equivalent combination of education and relevant experience. Certification not requiredPreferred Skills IATA Dangerous Goods handling—if not previously certified will train after hire. Prior lab experience including sample processing and shipping experience. Comfortable using Microsoft Word and Excel and databases. 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 $42,700.00 - $89,000.00. 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.

Shift: Monday - Friday, 8:30 AM - 5:00 PM Location: Houston, Texas Role and Responsibilities Label, receive, and process samples (blood, urine, tissue, stool, etc.) for clinical trials per specific protocol guidelines to include logging samples into and out of the department. Request and receive tissue samples from outside pathology facilities. Send tissue blocks to vendor to have slides cut and ship these slides to the study’s lab. Label, receive, and process samples (blood, urine, tissue etc.) for clinical trials per specific protocol guidelines to include logging samples into and out of the department. Record all data in specified forms per clinical trial (paper and electronic) with accuracy and responsibility. Enter data into departmental database. Recognize discrepancies in the data on the samples and coordinate with the clinical staff to correct. Organize and store all reagents according to safety instructions. Maintain equipment and a clean and orderly lab environment. Restock lab consumables at the end of the day. Manage inventory of clinical trial supplies and kits as well as departmental supplies. Administrative functions include filing, scanning, copying, and emailing of work documents. Ship or store samples as per protocol before the end of the shift. Prepare all collection tubes and aliquots for the next day’s clinic with accuracy and responsibility. Other duties as assigned. Minimum Qualifications and Education Requirements Lab Assistant training or associate degree in the Sciences or an equivalent combination of education and relevant experience. Certification not requiredPreferred Skills IATA Dangerous Goods handling—if not previously certified will train after hire. Prior lab experience including sample processing and shipping experience. Comfortable using Microsoft Word and Excel and databases. 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 $42,700.00 - $89,000.00. 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™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen. Werden Sie Teil unserer Community von rund 86.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welche Rolle Sie bei IQVIA einsteigen, es erwartet Sie ein offenes, innovationsfreudiges Umfeld, in dem Sie sich viel bewegen können. Finden Sie heraus, wie Sie Ihre Talente und Ihre Leidenschaften bei IQVIA einbringen können. Im Bereich Commercial Engagement Services (CES) arbeiten wir eng mit unseren Life Sciences-Kunden zusammen und unterstützen sie mit flexiblen Vertriebs- und Personallösungen für nachhaltigen Erfolg am Markt. Dies umfasst insbesondere die Rekrutierung, das Training und die Steuerung des Vertriebsteams in Dienstleistungsprojekten bzw. in Arbeitnehmerüberlassung. Dabei differenzieren wir uns über integrierte Projektansätze entlang des IQVIA Lösungsportfolios, die wir individuell an die Kundenbedürfnisse anpassen und aus einer Hand anbieten. Für ein spannendes Projekt im Bereich Dermatologie suchen wir Pharmaberater (m/w/d) zum nächstmöglichen Zeitpunkt Im Gebiet: Hamburg, Lüneburg, Weyhe, Gartow Das sind Deine Aufgaben: Aufbau und Pflege von tragfähigen Kundenbeziehungen zu Dermatolog*innen in Klinik und Praxis Eigenständige Gebietsplanung und Umsetzung eines individuellen Businessplans in Einklang mit der nationalen Strategie Vermittlung der medizinisch-wissenschaftlichen Inhalte und strategischen Kernbotschaften zur Festigung und zum Ausbau der Marktposition und Wettbewerbsdifferenzierung Unterstützung bei der Identifikation geeigneter Patientengruppen und Diskussion praxisrelevanter Einsatzmöglichkeiten – stets im fachlichen Austausch mit den behandelnden Ärzt*innen Initiierung, Organisation und Durchführung von lokalen (auch digitalen) Fortbildungsveranstaltungen Repräsentation des Produkts auf regionalen und nationalen Fachkongressen Effektive Zusammenarbeit im crossfunktionalen Team (u.a. mit Regeneron, Business Relation Management, Medical Scientific Liaison) Entwicklung lokaler Netzwerke in enger Abstimmung mit medizinischen und strategischen Funktionen Nutzung digitaler Tools und Omni-Channel-Möglichkeiten im Sinne der Kundenbedürfnisse Kollegiale Zusammenarbeit im regionalen und im Zentrumsteam Bereitschaft, sich in neue Indikationen einzuarbeiten und aktiv zur Marktentwicklung beizutragen Das bringst Du mit: Du hast bereits Erfahrung als Pharmaberater, Pharmareferent in verschiedenen Indikationen gesammelt, vorzugsweise in der Dermatologie Du verfügst über eine Naturwissenschaftliche Ausbildung (idealerweise Hochschulabschluss) oder Ausbildung zum Geprüften Pharmareferent (m/w/d) gemäß §75 AMG Als durchsetzungsstarke Persönlichkeit und erfahrener Netzwerker verstehst Du es, dich und Deine Ansprechpartner zu begeistern Du möchtest etwas bewegen – für Dein Präparat, für dich selbst und vor allem für betroffene Patienten Ausgeprägte kommunikative Fähigkeiten sowie die Bereitschaft, eigenverantwortlich und ergebnisorientiert zu arbeiten Teamfähigkeit und Fähigkeit zur transversalen Zusammenarbeit Deutschkenntnisse auf muttersprachlichem Niveau Gute Englischkenntnisse (für Fachliteratur) wünschenswert Das erwartet Dich bei uns: Ein attraktives Gehaltspaket plus Kundenprämien, vielfältige Corporate Benefits, betriebliche Altersvorsorge sowie 24/7 Unfallversicherung (auch für den privaten Bereich) und exklusive private Krankenzusatzversicherungen Ein top ausgestatteter Firmenwagen verschiedener Premiumanbieter mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des Modells Eine moderne IT-Ausstattung für Deinen modernen digitalen Arbeitsplatz Unser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige Perspektive Wir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines Wohnorts Eine hohe Übernahmequote durch unsere Kunden ermöglicht Dir den Karrierestart bei zukunftsweisenden und führenden Unternehmen der Pharmabranche und Medizintechnik-Branche Vielfältige und individuelle Weiterentwicklungsmöglichkeiten auch innerhalb von IQVIA (z.B. Führung, Key Account Management, Projektmanagement und vieles mehr) Wir begleiten Dich während Deiner Bewerbungsphase durch individuelle Betreuung/Vorbereitung bis zur Einstellung und auch darüber hinaus während des Beschäftigungsverhältnisses Unser Kunden-Netzwerk reicht vom Start-up Unternehmen bis zum Global Player. Gemeinsam mit Dir finden wir den richtigen Job für Dich! Starte Deine Karriere mit IQVIA! Dein besonders schneller Draht zu uns: Kandidaten-Hotline: 0621-84508113 oder sende uns gerne direkt Deine Bewerbung per Mail an: [email protected] #LI-CES #LI-DNP #LI-SS2 #Pharmaberater #Biologie #Chemie #Pharmareferent #BTA #CTA #PTA #Oecotrophologie #Pharmazie #Pharma-Außendienst IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Join IQVIA as a Clinical Research Associate 2 / CRA 2 or as Senior Clinical Research Associate 1 / SrCRA 1 (m/w/d) and work home-based throughout Germany in our single sponsor department. You will enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our clients. Whether you're just starting out or looking to deepen your expertise, this role promises to offer intentional career growth and professional development. With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas. Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits.Supporting the development of a subject recruitment plan.Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution.Collaborating with experts at study sites and with client representatives.Depending on client model there might be remote-monitoring, involvement in study start-up processes, specialization on therapeutic area (pharmaceutical product or medical devices).  Mentoring of less experienced team members, support as subject matter expert for specific topics or additional tasks might be included.Qualifications: University Degree in life science or other scientific discipline or apprenticeship in the health care field.Minimum of two-four years of on-site monitoring experience alternatively an equivalent combination of education, training and experience.Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.Strong written and verbal communication skills, attention to detail and ability to work in a fast pace environment.Fluency in German on at least C1 level and a good command of English.Flexibility to travel up to 40-60% of working time.Driver’s license class B.What you can expect: Permanent employment contract.Home-office and flexible working schedules.Competitive salaryCompany car or car allowance, accident insurance, pension and more.Resources that promote your career growth.Whatever your career goals, we are here to ensure you get there! Please apply with your English CV and motivation letter as well as your education certificates and job reference letters (Arbeitszeugnisse). 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.

Clinical Pharmacist Type: Full-time, hybrid We are looking for pharmacists to join the team! Join us in this exciting role where you will utilise your clinical expertise and commercial acumen to support patients with chronic conditions in primary care settings. As a clinical pharmacist at Interface Clinical Services, an IQVIA business, your responsibilities will include aiding practices with clinical tools, identifying opportunities for clinical reviews, ensuring adherence to protocols, and fostering awareness of Interface Clinical Services within primary care settings.  This is the perfect role for a pharmacist who is looking for career progression! Some principal responsibilities: Support Practices to provide clinical tools and resource to help manage patients with long-term conditions. To ensure clinical services are delivered within the bounds of our protocols, service operating instructions and systems. To identify opportunities for clinical reviews at individual practice level, PCN or ICB level where there is clinical need. To enhance the awareness of Interface Clinical Services within primary care and to assist in developing long lasting relationships with practices and local NHS organisations. Ideal candidate: Must be a GPhC registered pharmacist with a minimum of 2 yrs PQE MPharm essential. CPPE / PCPEP desirable. Community or primary care experience desirable. Willing to travel as required, along with remote (home) working. A keen passion to make a positive difference to patients’ long-term health. Driven work ethic. Benefits of working as Clinical Pharmacists with IQVIA: Funding and paid leave for the Independent Pharmacist Qualification. Access to learning and career path development tools. Become a clinical expert in long term conditions eg AF, asthma, COPD, diabetes, heart failure. Car allowance £5500 (PLUS paid mileage). 25 days annual paid holiday, NO weekend, bank holiday or evening working. Opportunity to buy extra 5 days annual leave. Competitive open-ended bonus. Private healthcare (BUPA). Flexible benefits including private dental, competitive pension scheme, Life Assurance, Group Income Protection, Personal Accident Insurance and more! Online wellbeing support available 24 hours a day, 7 days a week, 365 days a year. Other benefits at corporate rates such as: gym memberships, access to 100s of restaurant/store discounts. Regular remote coffee mornings, regional meetings / team social events. Manage your own diary to enable flexible working and in practice. Be part of the team and apply today! Interface Clinical Services, an IQVIA business, are the largest organisation within the UK healthcare sector to fully employ a team of pharmacists. We operate in partnership with both the NHS and industry. As pioneers of Clinical Pharmacist-led services, here at Interface we believe that a career in healthcare is more than just a job, it’s a vocation. Our mission is simple, to improve clinical outcomes and improve patients’ lives, we want you to be part of that journey and know that you are making a difference. Please note: Sponsorship is not available for this opportunity #LI-DNI #LI-CES #LI-SJ1 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:Performs quality control and editing review of Medical Writing deliverables from internal and external authors to ensure accuracy, consistency, and compliance with data, format, and style requirements. Provides leadership, training, and guidance to staff, and assists in resource management.Essential Functions: Is a subject- matter expert within the group and a source of advice and information to IQVIA staff on quality control processesConduct quality control (QC) review of a wide range of Medical Writing deliverables for both internal and external customers, including complex and substantial documents, with limited guidance and consistent high quality and efficiencyDocument findings clearly, in accordance with defined procedures and checklistsLiaise promptly with document authors in case of questions or missing sourcesDevelops quality tools such as checklists, quality guidelines, and standards to meet project specific needsMay have responsibility for resourcing of QC tasks within the teamTake a leading role in providing training, guidance, and mentoring within the QC groupMay take a formal supervisory role in managing QC staff and/or contract resourcesTake a leading role in proposing, developing, evaluating, and implementing process changes and tools and monitoring their adoption and benefitsTake a leading role in QC team meetings and ensuring that lessons learned are shared and consistent approaches are appliedMay take a leadership role for a stand-alone QC project, lead the team, and be the primary contact with the customerMay participate in project team meetings and liaise directly with the customer on QC issues, as appropriate and with senior support as neededTake responsibility for on-time delivery of QC review commentsManage daily assignments, planning and directing work, and take responsibility for managing workload for assigned projects and tasks, in collaboration with senior staffKeep abreast of current data, trends, medical writing (MW)/regulatory knowledge, developments and advances in area of drug development/MWQualifications: Bachelor's Degree in English or Life sciences -related discipline or related fieldTypically, at least 4 years experience working with clinical trial documentation in a research environment, including significant experience of performing quality control (QC) review of clinical trial-related documents, defining and refining processes, and training and developing othersRequires in-depth understanding of the structure, format, and purpose of a wide range of Medical Writing deliverables and the importance of consistency, clarity, and accuracy versus sourcesCareful attention to detail, accuracy, and consistencyImpeccable English language skills and ability to detect and correct grammatical, spelling, and language errorsAbility to understand scientific/medical documents and identify deficiencies, errors and inconsistenciesFamiliarity with the structural and content requirements of clinical study reports, investigator brochures, protocols, and similar documentsProactivity and advanced organizational and time management skills and ability to prioritize workload effectively with commitment to deadlinesAbility to communicate clearly, concisely, and effectively in English, both in writing and verbally, and confidence in using a range of communication methods to achieve resultsGood understanding of clinical drug development and the functions, steps, and processes involvedAdvanced understanding of the nature and purpose of Medical Writing deliverablesAbility to provide clear and effective guidance and training in the form of written instructions, presentations, and one-to-one discussionConfident use of Microsoft Office and Adobe AcrobatAbility to quickly establish and maintain effective working relationships with co-workers, managers, and customers at a range of seniority levelsTechnical Skills: Veeva VaultMicrosoft Office (Word, Excel, Power Point, etc.) (see above)Adobe Acrobat (see above)ISIToolboxSharePointExperience with publishing/submission-readiness a plusIQVIA 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 $84,400.00 - $211,100.00. 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.

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in CNS, GLP-1/Obesity/Diabetes (Type II) and/or Cardiovascular clinical trials. Phase 1 experience is a plus! Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.• Collaborate and liaise with study team members for project execution support as appropriate.• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.• If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Qualifications• Bachelor's Degree in scientific discipline or health care preferred. Req• Requires at least 1 year of on-site monitoring experience. Req• Equivalent combination of education, training and experience may be accepted in lieu of degree. Req• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).• Good therapeutic and protocol knowledge as provided in company training.• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).• Written and verbal communication skills including good command of English language.• Organizational and problem-solving skills.• Effective time and financial management skills.• 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 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 $71,900.00 - $189,000.00. 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 is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH, dermatology and/or asthma/respiratory clinical trials. Women's Health experience is a plus! Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.• Collaborate and liaise with study team members for project execution support as appropriate.• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.• If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Qualifications• Bachelor's Degree in scientific discipline or health care preferred. Req• Requires at least 1 year of on-site monitoring experience. Req• Equivalent combination of education, training and experience may be accepted in lieu of degree. Req• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).• Good therapeutic and protocol knowledge as provided in company training.• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).• Written and verbal communication skills including good command of English language.• Organizational and problem-solving skills.• Effective time and financial management skills.• 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 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 $71,900.00 - $189,000.00. 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.