IQVIA

Join a high-growth team at the forefront of eCOA delivery, where you’ll lead complex, global clinical programs that directly impact patient-centric research. As an Associate Director, you’ll take on a highly visible leadership role—driving project excellence, mentoring teams, and shaping operational strategy in a dynamic and evolving environment. Job Overview The Associate Director, eCOA Project Management is responsible for leading complex eCOA programs, ensuring successful delivery across scope, timeline, and quality expectations. This role combines hands-on project leadership, people management, and process improvement, with accountability for both project execution and team performance. You will oversee project managers, support escalations, contribute to account leadership activities, and drive operational excellence across the portfolio. The role is remote with occasional travel and a preference for Eastern Time Zone alignment. Key Responsibilities Define and validate project/program scope, timelines, and success metrics for complex eCOA implementationsLead end-to-end project delivery, including scope, schedule, cost, and quality managementIdentify risks and develop mitigation strategies; track and report portfolio performanceManage and mentor a team of project managers (approximately 7–8 direct reports)Conduct regular one-on-ones, manage performance, and support career development of team membersAct as first point of escalation for project and team-related issuesSupport account leadership and client deliverables as neededPartner with stakeholders to ensure alignment on project goals and outcomesLead or contribute to process improvement initiatives and SOP developmentDrive change management, including training coordination and onboarding of new team membersDeliver presentations and communicate project updates to leadership and cross-functional teamsQualifications Bachelor’s degree in Computer Science, Life Sciences, or a related field (or equivalent experience)Approximately 5+ years of direct people management experience preferredStrong project management experience in clinical technology or eCOA (preferred but not required if project management expertise is strong)Demonstrated experience managing complex programs and cross-functional teamsExcellent communication and presentation skills (including PowerPoint, Teams, and stakeholder engagement)Ability to manage multiple priorities in a fast-paced, evolving environmentNice to Have eCOA systems experienceFamiliarity with IRT or eConsent platformsIQVIA 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 $100,200.00 - $278,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Senior Software Architect (m/w/d) full remote Dortmund / Vollzeit (in Gleitzeit) Health System Services (HSS) wurde 1990 gegründet und ist einer der führenden Technologieanbieter und Dienstleister im deutschen Gesundheitsmarkt. Zu den Schwerpunkten unserer Tätigkeit gehören das Genehmigungs- und Abrechnungsmanagement, die Softwareentwicklung und -bereitstellung sowie Digitalisierungs- und Archivierungsleistungen für Krankenkassen. Wir suchen dich für unseren Geschäftsbereich in Dortmund mit rund 170 Mitarbeitenden. Für unsere Kunden aus dem Bereich Healthcare entwickeln wir Software zur Digitalisierung von Geschäftsprozessen von der Architektur bis zur Implementierung. Dabei setzen wir auf Standard-Technologien, verlieren aber auch neue Entwicklungen nicht aus dem Auge. Bei uns arbeitest du im dynamischen Umfeld eines IT-Unternehmens mit aktuellen Technologien und IT-Systemen. Deine AufgabenWeiterentwicklung und Umsetzung der Unternehmensarchitektur mit internationalen Teams Konzeption von Architekturstrategien und Abstimmung mit Management und Architekturboard Organisation, Moderation und Nachverfolgung von Architektur-Entscheidungen Beratung des Managements sowie Priorisierung von Projekten gemeinsam mit dem Produktmanagement Analyse bestehender Systeme und Entwicklung innovativer Softwarelösungen Förderung moderner Technologien, agiler Methoden und Engineering-Standards Sicherstellung der Einhaltung von Architekturprinzipien, Richtlinien und regulatorischen Vorgaben Enge Zusammenarbeit mit internen und externen Stakeholdern in einem internationalen Umfeld Förderung von Mitarbeitenden sowie aktive Begleitung von Veränderungsprozessen Dein ProfilAbgeschlossenes Studium der Informatik oder eine vergleichbare Qualifikation Mindestens 5 Jahre Berufserfahrung in der Softwareentwicklung, idealerweise im Gesundheitswesen oder öffentlichen Sektor Sehr gutes Verständnis moderner Softwarearchitekturen und Entwicklungsmethoden (z. B. SOA, APIs, Cloud, CI/CD) Erfahrung mit agilen Methoden wie Scrum oder Kanban Idealerweise Kenntnisse regulatorischer Anforderungen im Gesundheitswesen sowie Erfahrung in internationalen Teams Ausgeprägte Kommunikationsstärke, Empathie und soziale Kompetenz Fähigkeit, Teams zu motivieren und technische wie fachliche Perspektiven zu verbinden Selbstständige, strukturierte und lösungsorientierte Arbeitsweise mit hoher Verantwortungsbereitschaft Sehr gute Deutsch- und Englischkenntnisse Souveränität im Umgang mit Konflikten, Feedback und Entscheidungsprozessen Du profitierst unter anderem von diesen Benefits: Flexible Arbeitszeiten im Gleitzeitmodell und full remote / anlassbezogen im Büro 30 Tage Urlaub pro Jahr Kostenfreie Nutzung der LinkedIn Learning Plattform Individuelle Weiterbildungsmöglichkeiten und regelmäßige Feedbackgespräch Betriebliche Altersvorsorge Fitnessbereich und Lounge mit Kicker und Spielekonsole im Büro Teamevents und Firmenfeste kostenlose Kalt- & Heißgetränke Wir schätzen Vielfalt und begrüßen daher alle Bewerbungen – unabhängig von Geschlecht, Nationalität, ethnischer und sozialer Herkunft, Religion/Weltanschauung, Behinderung, Alter sowie sexueller Identität IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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 88.000 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. Dazu gehören integrierte Projektansätze entlang unseres IQVIA-Lösungsportfolios, die wir individuell an Kundenbedürfnisse anpassen und aus einer Hand anbieten. Für einen bundesweiten Teamaufbau in der Dermatologie suchen wir erfahrene Pharmaberater im Facharztaußendienst (m/w/d) ab dem 01.06.2026 im Gebiet: Dresden, Bautzen, Görlitz, Cottbus Rollenbeschreibung Primärer kommerzieller Ansprechpartner für zugewiesene dermatologische Key Accounts Aufbau langfristiger, vertrauensvoller Beziehungen zu Dermatologen und relevanten Praxis-Stakeholdern Positionierung des Produkts als differenzierte Therapieoption innerhalb bestehender Behandlungswege Umsetzung der nationalen Launch-Strategie in individuelle, maßgeschneiderte Account-Pläne Sicherstellung einer schnellen Marktdurchdringung in der frühen Post-Launch-Phase Durchführung hochwertiger wissenschaftlicher und wertbasierter Gespräche Gesamtverantwortung für die Gebietsperformance und regionale Geschäftsergebnisse Anwendung strukturierter Account-Planung und Priorisierung Nutzung von Daten und Insights zur Optimierung der Kundeninteraktion Enge Zusammenarbeit mit funktionsübergreifenden kommerziellen und medizinischen Teams Arbeiten innerhalb klar definierter Compliance- und Governance-Richtlinien Auftreten als professioneller Markenbotschaften Erforderliche Qualifikationen Ein abgeschlossenes Studium (z. B. pharmazeutische Wissenschaften, Naturwissenschaften) oder eine vergleichbare Qualifikation nach §75 AMG. Erfahrung im pharmazeutischen Spezialaußendienst, idealerweise im Bereich Dermatologie Fundiertes Verständnis des deutschen Gesundheitssystems Gültiger Führerschein sowie Reisebereitschaft innerhalb des jeweiligen Gebiets Verhandlungssichere Deutschkenntnisse (C1–C2) Erforderliche Erfahrung Idealerweise Erfahrung mit Produkteinführungen oder Indikationserweiterungen Erfahrung im Management von Key Accounts im Specialty-Care-Bereich, bevorzugt Dermatologie Anwendung von CRM-Systemen und strukturierten Vertriebsprozessen Erfahrung in Matrix- oder Outsourcing-Umfeldern (von Vorteil) Zentrale Fähigkeiten & Kompetenzen Positive, lösungsorientierte Denkweise mit hoher intrinsischer Motivation Exzellente Kommunikationsfähigkeiten – klar, überzeugend und verlässlich Ausgeprägte Kundenorientierung und starkes Account-Mindset Proaktive, antreibende Persönlichkeit mit hoher Eigenverantwortung Hohe Umsetzungsstärke und Belastbarkeit Analytische und insight-getriebene Arbeitsweise Erfahrung und Begeisterung für funktionsübergreifende Zusammenarbeit Teamplayer mit Kompetenz im Stakeholder-Management und in der interdisziplinären Zusammenarbeit Affinität zu Multichannel-Selling sowie modernen digitalen Interaktionsformaten 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 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 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 #PharmaceuticalSales #KAM #PharmaRepresentative #Pharmacy #FieldSales #Dermatology IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA™ – 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 88.000 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. Dazu gehören integrierte Projektansätze entlang unseres IQVIA-Lösungsportfolios, die wir individuell an Kundenbedürfnisse anpassen und aus einer Hand anbieten. Für einen bundesweiten Teamaufbau in der Dermatologie suchen wir erfahrene Pharmaberater im Facharztaußendienst (m/w/d) ab dem 01.06.2026 im Gebiet: Dortmund, Hagen, Hamm, Lüdenscheid     Rollenbeschreibung Primärer kommerzieller Ansprechpartner für zugewiesene dermatologische Key Accounts Aufbau langfristiger, vertrauensvoller Beziehungen zu Dermatologen und relevanten Praxis-Stakeholdern Positionierung des Produkts als differenzierte Therapieoption innerhalb bestehender Behandlungswege Umsetzung der nationalen Launch-Strategie in individuelle, maßgeschneiderte Account-Pläne Sicherstellung einer schnellen Marktdurchdringung in der frühen Post-Launch-Phase Durchführung hochwertiger wissenschaftlicher und wertbasierter Gespräche Gesamtverantwortung für die Gebietsperformance und regionale Geschäftsergebnisse Anwendung strukturierter Account-Planung und Priorisierung Nutzung von Daten und Insights zur Optimierung der Kundeninteraktion Enge Zusammenarbeit mit funktionsübergreifenden kommerziellen und medizinischen Teams Arbeiten innerhalb klar definierter Compliance- und Governance-Richtlinien Auftreten als professioneller Markenbotschaften Erforderliche Qualifikationen Ein abgeschlossenes Studium (z. B. pharmazeutische Wissenschaften, Naturwissenschaften) oder eine vergleichbare Qualifikation nach §75 AMG. Erfahrung im pharmazeutischen Spezialaußendienst, idealerweise im Bereich Dermatologie Fundiertes Verständnis des deutschen Gesundheitssystems Gültiger Führerschein sowie Reisebereitschaft innerhalb des jeweiligen Gebiets Verhandlungssichere Deutschkenntnisse (C1–C2) Erforderliche Erfahrung Idealerweise Erfahrung mit Produkteinführungen oder Indikationserweiterungen Erfahrung im Management von Key Accounts im Specialty-Care-Bereich, bevorzugt Dermatologie Anwendung von CRM-Systemen und strukturierten Vertriebsprozessen Erfahrung in Matrix- oder Outsourcing-Umfeldern (von Vorteil) Zentrale Fähigkeiten & Kompetenzen Positive, lösungsorientierte Denkweise mit hoher intrinsischer Motivation Exzellente Kommunikationsfähigkeiten – klar, überzeugend und verlässlich Ausgeprägte Kundenorientierung und starkes Account-Mindset Proaktive, antreibende Persönlichkeit mit hoher Eigenverantwortung Hohe Umsetzungsstärke und Belastbarkeit Analytische und insight-getriebene Arbeitsweise Erfahrung und Begeisterung für funktionsübergreifende Zusammenarbeit Teamplayer mit Kompetenz im Stakeholder-Management und in der interdisziplinären Zusammenarbeit Affinität zu Multichannel-Selling sowie modernen digitalen Interaktionsformaten 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 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 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 #PharmaceuticalSales #KAM #PharmaRepresentative #Pharmacy #FieldSales #Dermatology IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

We are seeking Project Manager, Project Services to join IQVIA Laboratories at Buenos Aires, Argentina.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Job Summary:Responsible for leading Project Management operational delivery for complex clinical research studies while serving as a key point of contact for internal and external stakeholders. Drives study setup, execution, and continuous improvement to ensure high-quality delivery aligned with customer and regulatory expectations. What You'll Be Doing:Lead study setup activities including protocol and budget review, project planning, and risk managementManage complex clinical studies across multiple regions, ensuring high-quality database setup and documentation readinessMonitor study progress, timelines, and deliverables while maintaining accurate documentation within eTMF systemsAct as primary customer contact, building strong relationships and leading meetings, presentations, and governance activitiesOversee study scope, budget, and quality, implementing corrective actions and sharing lessons learnedCoordinate cross-functional teams and serve as escalation point for study and program-level issuesProvide training to sites, CRAs, and customers, while mentoring junior team membersSupport process improvements, audits, inspections, and may lead global customer programs What We Are Looking For:Bachelor's Degree Life Sciences or related field preferred5+ years of clinical or research industry experience, including 3-year project management / project set up experience preferredThorough knowledge of Project Management processes and central laboratory operations (kits/supplies, logistics, specimen storage, data reporting and transfers)Demonstrated computer proficiency with Microsoft Office and experience with centralized laboratory systems or equivalentOther equivalent combination of education, training, and experience may be accepted in lieu of degree The Knowledge, Skills and Abilities Needed for This Role:Excellent interpersonal and customer relationship management skillsStrong organizational skills with the ability to manage multiple priorities in a fast-paced environmentEffective written and verbal communication skills with strong command of the English language What We Offer You:We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey. To learn more about our benefits, visit https://jobs.iqvia.com/benefits. If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is 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.

Buscamos un candidato con buena predisposición para aprender y excelente capacidad de análisis, actual estudiante de carrera de grado, que desee realizar su práctica profesional en nuestra empresa para el equipo de PBS en la compañía. Principales responsabilidades: Revisión de datos la mejora de los registrosCruce de información de médicosRevisión de Obras SocialesSupervisar, verificar, depurar y analizar información que recopila aplicación de desarrollo interno que recolecta inormacion de web para armar nuestras bases de datos médicasContamos con una aplicación de desarrollo interno que recolecta información de la web para armar nuestras bases de datos médicas y buscamos una persona que pueda supervisar, verificar, depurar y analizar la información que recopila, mejorando así la calidad integral, para poder ofrecer un mejor servicio a nuestros clientes. Requisitos clave: Estudiante de carrera de gradoMínimo 1,5 años restante (no próximo a graduarse)Inglés intermedioEstudiante de carreras: Sistemas / Ingeniería, Administración, Marketing, AfinesIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

We are seeking a Senior Project Services Coordinator to join IQVIA Laboratories at Argentina.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development.Job Summary:Provide day-to-day operational support to the Project Manager and study team by completing routine project procedures across the full study lifecycle, from start-up through close-out. Ensure all work is performed in line with standard operating procedures, policies, and good practices.What You'll Be Doing:Support study setup and planning by attending meetings, preparing minutes and action logs, and drafting protocol-specific laboratory instruction documentsUnder Project Manager supervision, help set up protocol-specific Laboratory Centralized Monitoring requirementsPerform routine study maintenance tasks including site loading, Investigator Portal access support, kit shipment coordination, and monitoring day-to-day study performancePartner with internal and external teams to drive timely resolution of queries, protocol questions, issues, and escalationsUse status reports and monitoring outputs to proactively identify trends and provide feedback on investigator site performance and service deliverySupport document quality control reviews and contribute to monitoring plans, reports, and protocol-specific materialsCoordinate stakeholder communications and lead customer communications when the Project Manager is absentSupport project close-out activities and contribute to process improvement initiatives, SOP updates, and ad hoc high-priority tasksWhat We Are Looking For:High School Diploma or equivalent required; Bachelor’s Degree in life sciences or related field preferred1 year of experience coordinating studies in a clinical research environment1 year of experience in project management methodologiesExperience using investigator portals and study tracking/status reporting tools to monitor study performance and site activityProficiency with Microsoft Word, PowerPoint, and Excel (word processing, presentations, and spreadsheets)Other Equivalent combination of education, training, and experience may be accepted in lieu of degreeThe Knowledge, Skills and Abilities Needed for This Role:Strong interpersonal and communication skills, including strong written and verbal EnglishExcellent organizational and time management skills with the ability to handle multiple competing prioritiesDemonstrated critical thinking and problem-solving skills, with the ability to work effectively in a fast-paced, high-stress environmentWhat We Offer You:We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.To learn more about our benefits, visit https://jobs.iqvia.com/benefits.If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

We are seeking an External Laboratory Network Lead to join IQVIA Laboratories at Buenos Aires, Argentina.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development.Job Summary:Under general direction, manage all aspects of work performed at third-party laboratories for assigned clinical trial projects. Serve as the primary point of contact, ensuring sample processing, sample handling, and data delivery meet study requirements throughout the full study lifecycle.What You'll Be Doing:Act as the primary liaison between external laboratories and internal project teams to coordinate study-level activitiesManage study startup, maintenance, and closeout activities including Work Order creation and executionEnsure accurate test information, pricing alignment, and metadata collection including test codes and specificationsOversee sample processing and sample handling activities to ensure compliance with study protocols and timelinesSupport data flow processes including data imports, query resolution, and collaboration with Data ManagementInvestigate quality issues, perform root cause analysis, and support CAPA development with internal and external stakeholdersProvide ongoing study support and contribute to financial reconciliation and invoice processingWhat We Are Looking For:Bachelor's Degree in Life Sciences and/or related field preferred2-3 years of experience in clinical trials/ hospital-funded research, project management or laboratory environment preferredWorking knowledge of central laboratory operations including sample logistics, specimen storage, and data reportingProficiency in Microsoft Office and experience with centralized laboratory or clinical systemsOther Equivalent combination of education, training, and experience may be accepted in lieu of degreeThe Knowledge, Skills and Abilities Needed for This Role:Strong interpersonal and vendor management skills with the ability to build effective working relationshipsDemonstrated organizational skills with ability to manage multiple priorities in a fast-paced environmentStrong written and verbal communication skills with good command of the English languageWhat We Offer You:We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.To learn more about our benefits, visit https://jobs.iqvia.com/benefits.If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is 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 Manager – Sponsor Dedicated. Clinical Project Management services provide management of a clinical trial (s) in a local level. Services/deliverables include operational oversight of assigned project(s) at the local level for end-to-end project management from start-up through to closeout activities. Tasks & Responsibilities: • Services rendered will adhere to applicable Sponsor SOPs, WIs, policies, codes of Good Clinical Practice (GCP), local regulatory requirements. • Prepares or contributes to high level budget estimate in response to Request for Service’s followed by detailed budget proposal. Ensures overall contract management, including review and approval of external service provider (ESP) contracts, change orders and ensures services are delivered per contract. • Act as primary company contact for assigned trial at the country level and ensures local/country team is tracking project progress against planned timelines and monitors patient recruitment rate to ensure that target enrollment will be met across the allocated countries. This may require development of local trial specific procedures and tools, recruitment planning, contingency and risk management, and budget forecasting. • Drive study compliance by maintaining and updating trial management systems, using study tools and management reports available to analyze trial progress. Participates in preparation for and conduct of Health Authority (HA) inspections and internal Quality Assurance audits. Escalates corrective and preventive actions (CAPA) to GTL MAO and CPL when the trial deviates from plans and communicates study progress and issues to study management teams and business partners. • Contributes to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research target. • Contributes to patient understanding of protocol and patient safety by contributing to the review of country specific informed consent in accordance with procedural document/templates. This includes reviewing and managing site specific informed consent forms in accordance with SOPs, other procedural documents and applicable regulations. Essentials Requirements: • BA/BS degree. • Degree in a health or science related field. • Minimum of 2 years of local/regional trial management experience in the pharmaceutical industry or CRO and previous experience as Clinical Research Associate. • Specific therapeutic area experience may be required depending on the position. • Strong working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures. • Strong IT skills in appropriate software and company systems. Willingness to travel with occasional overnight stay away from home according to business needs. • Excellent decision-making and string financial management skills. • Proficient in speaking and writing the country language and English. Good written and oral communication skills as appropriate. 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 OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.Home Based opportunity requiring experience with local submissions and contracts. Fluency in Polish language.   Essential Functions Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines. Perform start up and site activation activities according to applicable regulations, SOPs and work instructions. Distribute completed documents to sites and internal project team members. Prepare site regulatory documents, reviewing for completeness and accuracy. Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information. Review and provide feedback to management on site performance metrics. Review, establish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as needed. Inform team members of completion of regulatory and contractual documents for individual sites. Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines. Provide local expertise to SAMs and project team during initial and on-going project timeline planning. Perform quality control of documents provided by sites. May have direct contact with sponsors on specific initiatives. QualificationsBachelor’s Degree in life sciences or a related field and 3 years’ clinical research or other relevant experience; or equivalent combination of education, training and experience. In-depth knowledge of clinical systems, procedures, and corporate standards. Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines. Knowledge of applicable regulatory requirements, including local regulations, SOPs and company’s Corporate Standards. Understanding of regulated clinical trial environment and knowledge of drug development process. Ability to establish and maintain effective working relationships with coworkers, managers and clients. In today’s world, continuing to grow and expand your skills is as important as ever. Discover career possibilities and chart your own path at IQVIA. The potential base pay range for this role, when annualized, is 11,463,500 HUF - 17,195,300 HUF. 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. Employee Referral Payment Standard Referral Bonus Plan 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.

As a global leader in commercial solutions, IQVIA is uniquely positioned to deliver results both nationally and internationally. Our teams partner with biopharma companies to bring essential medicines to the people who need them most. We empower our clients with insights and access to their markets, helping them demonstrate the value of their products to payers, physicians, and patients alike. A core part of our mission includes serving as the sales force for biopharma or providing nurse educators who support patients and prescribers. With the right experience, you can help bring medical innovations to life in real-world settings. We’re excited to announce an opportunity to join our team of over 10,000 field professionals worldwide—we’re currently hiring a Nurse Educator to support our pharmaceutical and biotech clients. Nurse Educator At the heart of our business strategies is a commitment to patients. The Nurse Educator Program is a patient-centered, educational initiative designed to support individuals living with chronic conditions who have been prescribed specific therapies. Nurse Educators play a vital role in helping patients understand their treatment, manage their condition, and access relevant resources related to their prescribed medication. This role involves one-on-one engagement with patients through various channels, including in-person visits, phone calls, video conferencing, email, and SMS—always in strict alignment with program guidelines. Please note: this is an educational role only. Nurse Educators do not provide clinical care or medical advice. Role Overview: Nurse Educator As a Nurse Educator, you will play a key role in supporting patients by connecting them with program-approved resources and delivering personalized education on chronic disease management and prescribed therapies. This role is designed to empower patients, promote treatment adherence, and encourage meaningful dialogue with healthcare providers. Key Responsibilities Facilitate connections between patients and approved educational resources. Deliver direct, disease-specific education and training related to prescribed medications. Support multiple disease states and therapies as needed. Promote behavioral change through patient-centered education to improve treatment adherence. Encourage effective communication between patients and their healthcare providers. Qualifications Bachelor’s degree and/or BSN preferred. Active RN license in state of residence; compact multi-state license preferred where applicable. Nursing license must be current and in good standing. Minimum of 5 years of clinical experience in healthcare (hospital, home health, pharmaceutical, or biotech settings). Prior experience as a nurse educator is preferred. Bilingual in English and Spanish is a plus. Valid driver’s license required. Must reside within the designated territory. Experience in direct patient interaction with a focus on adherence and persistence. Strong understanding of clinical data and pharmacology. Excellent time management, planning, and multitasking skills. Effective presentation and motivational skills; strong interpersonal and communication abilities. Ability to work independently and cross-functionally. Dedicated home workspace required. Adaptability to changing responsibilities and environments. Proficiency in Microsoft Office (Word, Excel, PowerPoint) and iPad technology. Flexibility to work evenings and weekends as needed. Willingness to travel up to 60–70%. Compliance with client vaccination requirements may be necessary. Compensation Competitive annual salary Car allowance Bonus eligibility  #LI-CES IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is $95,000-$105,000 annually. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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 88.000 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. Dazu gehören integrierte Projektansätze entlang unseres IQVIA-Lösungsportfolios, die wir individuell an Kundenbedürfnisse anpassen und aus einer Hand anbieten. Für einen bundesweiten Teamaufbau in der Dermatologie suchen wir erfahrene Pharmaberater im Facharztaußendienst (m/w/d) ab dem 01.06.2026 im Gebiet: Bremen, Bremerhaven, Cuxhaven, Stade Rollenbeschreibung Primärer kommerzieller Ansprechpartner für zugewiesene dermatologische Key Accounts Aufbau langfristiger, vertrauensvoller Beziehungen zu Dermatologen und relevanten Praxis-Stakeholdern Positionierung des Produkts als differenzierte Therapieoption innerhalb bestehender Behandlungswege Umsetzung der nationalen Launch-Strategie in individuelle, maßgeschneiderte Account-Pläne Sicherstellung einer schnellen Marktdurchdringung in der frühen Post-Launch-Phase Durchführung hochwertiger wissenschaftlicher und wertbasierter Gespräche Gesamtverantwortung für die Gebietsperformance und regionale Geschäftsergebnisse Anwendung strukturierter Account-Planung und Priorisierung Nutzung von Daten und Insights zur Optimierung der Kundeninteraktion Enge Zusammenarbeit mit funktionsübergreifenden kommerziellen und medizinischen Teams Arbeiten innerhalb klar definierter Compliance- und Governance-Richtlinien Auftreten als professioneller Markenbotschaften Erforderliche Qualifikationen Ein abgeschlossenes Studium (z. B. pharmazeutische Wissenschaften, Naturwissenschaften) oder eine vergleichbare Qualifikation nach §75 AMG. Erfahrung im pharmazeutischen Spezialaußendienst, idealerweise im Bereich Dermatologie Fundiertes Verständnis des deutschen Gesundheitssystems Gültiger Führerschein sowie Reisebereitschaft innerhalb des jeweiligen Gebiets Verhandlungssichere Deutschkenntnisse (C1–C2) Erforderliche Erfahrung Idealerweise Erfahrung mit Produkteinführungen oder Indikationserweiterungen Erfahrung im Management von Key Accounts im Specialty-Care-Bereich, bevorzugt Dermatologie Anwendung von CRM-Systemen und strukturierten Vertriebsprozessen Erfahrung in Matrix- oder Outsourcing-Umfeldern (von Vorteil) Zentrale Fähigkeiten & Kompetenzen Positive, lösungsorientierte Denkweise mit hoher intrinsischer Motivation Exzellente Kommunikationsfähigkeiten – klar, überzeugend und verlässlich Ausgeprägte Kundenorientierung und starkes Account-Mindset Proaktive, antreibende Persönlichkeit mit hoher Eigenverantwortung Hohe Umsetzungsstärke und Belastbarkeit Analytische und insight-getriebene Arbeitsweise Erfahrung und Begeisterung für funktionsübergreifende Zusammenarbeit Teamplayer mit Kompetenz im Stakeholder-Management und in der interdisziplinären Zusammenarbeit Affinität zu Multichannel-Selling sowie modernen digitalen Interaktionsformaten 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 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 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 #PharmaceuticalSales #KAM #PharmaRepresentative #Pharmacy #FieldSales #Dermatology 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.

Site Activation Specialist Country Site Activation - CSA Slovakia - To support DACH region Homebased Make an impact on patient health! IQVIA’s Global Site Activation Team of 2000 employees, drives best in class site and customer experience, with industry leading outcomes. We keep the patient at the forefront; ‘Always Impatient for the Patient’ and we excel in our collaboration with our external/internal customers. IQVIA’s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication. We are leaders in innovation and first to new technologies, meaning a vast amount of career development opportunities are available. Job Overview: As a Site Activation Specialist, you will serve as a Single Point of Contact to perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager, Project Management team, and other departments as necessary. You will review documents for completeness, consistency, and accuracy, under guidance of senior staff and prepare site documents, inform team members of completion of regulatory contractual. Along with distributing completed documents to sites and internal project team member and updating and maintaining internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project specific information. You will also review, track, and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form, and Investigator Pack release documents. Requirements: Bachelor’s Degree in Life Science or related field Prior experience in Site Activation, Regulatory Submissions and/or Contract negotiation (or equivalent combination of education, training and clinical, healthcare and/or pharma experience) Ability to work independently but also collaborate with others Good interpersonal, communication and organisational skills to establish and maintain effective working relationships with co-workers, managers and sponsors Ability to work on multiple projects Knowledge of applicable functional/regulatory requirements, including local regulations, SOPs and ICH/ GCP German is required Unleash your potential! It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world. When you join our diverse, global team, you’ll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is €30,800.00 - €46,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Position SummaryThe Accounting Manager is responsible for overseeing general financial accounting operations, ensuring integrity and accuracy of financial data, and supporting monthly, quarterly, and annual close processes. This role manages day‑to‑day accounting activities, supervises team performance, ensures compliance with statutory, regulatory, and corporate accounting standards, and supports internal and external audits. The Accounting Manager also contributes to financial reporting, process improvements, and cross‑functional initiatives that strengthen financial governance and operational efficiency. Key ResponsibilitiesGeneral Accounting & Financial ReportingLead monthly, quarterly, and annual closing activities, ensuring timely and accurate general ledger maintenance.Prepare and review journal entries, reconciliations, and financial reports in accordance with corporate policies and relevant accounting standards.Ensure compliance with US GAAP, IFRS, and local statutory requirements (as applicable).Oversee the preparation of statutory accounts and support regulatory filing processes.Process Management & Continuous ImprovementDesign, implement, and optimize accounting processes, workflows, and controls.Ensure consistent application of accounting policies across the team and wider organization.Support and lead initiatives focused on automation, efficiency, and operational excellence.Team LeadershipManage, coach, and develop accounting staff; set priorities, monitor workload, and ensure timely execution of deliverables.Drive performance, accountability, and professional development within the team.Audit & ComplianceAct as primary contact for internal and external audit activities.Prepare audit schedules, respond to auditor inquiries, and ensure audit issues are addressed promptly.Maintain strong internal controls and ensure adherence to corporate compliance standards.Accounts Payable, Receivables & Treasury SupportOversee supplier invoice processing, payment execution, and related control activities.Support customer remittance processes, employee expense reimbursements, and cash flow management.Coordinate with Treasury, Tax, and other Finance stakeholders as needed.Cross‑Functional PartnershipCollaborate with Finance, Operations, HR, Legal, and other departments to provide financial insights and support business initiatives.Participate in project work, system enhancements, and process transitions.Required QualificationsExperienceMinimum 3–5 years of relevant accounting or financial management experience.Experience in general ledger accounting, financial reporting, and closing processes.Previous exposure to people leadership or supervisory responsibilities preferred.EducationBachelor’s degree in Accounting, Finance, Business Administration, or related field (Master’s degree or professional certification preferred).Knowledge & SkillsSolid understanding of accounting principles, financial controls, and reporting standards.Proficiency in management skills such as scheduling, prioritization, coaching, and workflow management.Strong analytical and problem-solving capabilities.Excellent communication, stakeholder management, and organizational skills.Experience working with ERP systems (SAP, Oracle, PeopleSoft, etc.); advanced Excel skills a plus.Certifications (optional / depending on region)CPA, ACCA, CMA, or equivalent professional certification preferred.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is €31,700.00 - €47,500.00. 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.

Credit ControllerUndertake Cash Collections across the Group including dispute resolutions, escalations. compliance with bad debt policy and adhoc tasks as required Job OverviewUnder supervision, provide routine accounting services to the business units and perform duties in accordance with IQVIA Finance Standard Operating Procedures (SOPs), Sarbanes-Oxley Controls and Unit Service Level Agreements (SLAs) (if applicable). Essential Functions• Input data accurately and within deadlines according to SOPs and Service Level Agreements (SLAs).• Contact employees and other departments as necessary to request missing information and update invalid data issues.• File appropriate documents.• Identify, track and report accounting data accurately and follow-up on routine issues flagging non standard issues to line manager.• Provide assistance to other team members including some guidance to junior team members, as required to ensure that the group meets all SLAs and targets.• Participate in teams handling various routine tasks within the accounting department.• Provide standard and ad hoc reports as needed.• Check that appropriate approvals are obtained for accounting purposes.• Flag problems with existing procedures and systems and make suggestions for improvements.• Perform other duties as assigned. Qualifications• High School Diploma or equivalent  Req• 4 years’ Finance experience Req Or• Equivalent combination of education, training and experience. Req• Knowledge of Peoplesoft Finance modules.• Knowledge of Microsoft Office applications.• Attention to detail.• Accurate and efficient data entry skills.• Ability to prioritize own workloads to meet deadlines.• Ability to establish and maintain effective working relationships with co-workers and managers. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

To be eligible for this position, you must reside in the same country/sales region where the job is located. About IQVIA Clinical & Patient Technology IQVIA™ is The Human Data Science Company™, focused on using data, technology, and advanced analytics to help life sciences organizations drive better outcomes for patients. IQVIA Clinical & Patient Technology plays a critical role in this mission by enabling faster, higher-quality, and more patient-centric clinical development through technology-enabled solutions. The Clinical & Patient Technology portfolio supports sponsors across the end-to-end clinical trial lifecycle, from study design and start-up through execution, close-out, and real-world impact. Solutions are CRO-, device-, and EDC-agnostic, interoperable within sponsor ecosystems, and designed to improve patient engagement, data quality, operational efficiency, and speed to insight. Role Overview The Senior Director, Sales – Large Pharma US, Clinical & Patient Technology is responsible for owning and driving total sales performance across the top US-based global pharmaceutical companies, with headquarters primarily located in the United States. This role has full accountability for revenue growth, strategic account development, and leadership of a team of Account Executives focused on the Large Pharma segment. The Senior Director will define and execute the go-to-market strategy, lead complex enterprise deals, and engage senior and C‑suite stakeholders to position IQVIA as a strategic clinical technology partner. Key Responsibilities Sales Leadership & Revenue Ownership Own total sales performance and revenue growth for the US Large Pharma segment within Clinical & Patient Technology. Lead, coach, and manage a team of Account Executives, ensuring consistent execution against revenue, pipeline, and growth objectives. Establish clear performance expectations, territory/account strategies, and development plans for the sales team. Drive accountability for forecast accuracy, pipeline health, and deal execution discipline. Strategic Account & Enterprise Sales Execution Personally lead large, complex, multi-year and multi-solution enterprise deals that are critical to achieving financial and strategic goals. Develop and execute comprehensive account strategies for top-tier global pharmaceutical customers headquartered in the US. Build and sustain executive-level relationships, including C‑suite and senior decision-makers across clinical, digital, data, procurement, and innovation organizations. Position IQVIA’s Clinical & Patient Technology portfolio as a strategic enabler of clinical execution, patient engagement, and operational transformation. Cross-Functional & Enterprise Collaboration Collaborate closely with marketing, operations, delivery, product, and solution strategy teams to align customer needs with IQVIA capabilities. Partner with broader IQVIA commercial and account teams to ensure a coordinated enterprise approach across large global customers. Provide market and customer insights to inform portfolio evolution, commercial strategy, and investment priorities. Market & Customer Expertise Maintain deep understanding of pharmaceutical R&D challenges, evolving regulatory complexity, and the role of technology in improving clinical trial execution. Anticipate customer needs and shape opportunities across eCOA, patient engagement, decentralized trial components, data and analytics, and integrated clinical technology solutions. Represent IQVIA as a trusted thought partner with senior sponsor organizations. Required Qualifications Experience & Domain Expertise Minimum 5 years of experience in a senior sales leadership role within Clinical Technology, Clinical Operations technology, or closely related Life Sciences technology domains. Demonstrated domain knowledge of clinical trials, patient engagement technologies, and sponsor-driven technology adoption models. Proven track record of successfully selling complex technology portfolios into large global pharmaceutical companies. Prior experience selling a similar Clinical & Patient Technology portfolio into the same or comparable Large Pharma US accounts. Established senior-level and executive relationships within major pharmaceutical organizations. Experience managing or contributing to global or multi-country strategic accounts. Sales Leadership & Management Skills Demonstrated ability to lead, motivate, and scale high-performing sales teams. Strong experience with enterprise sales cycles, complex negotiations, and multi-stakeholder decision processes. Excellent forecasting, pipeline management, and revenue ownership discipline. Outstanding negotiation skills with the ability to close high-value, strategic deals. Executive Presence & Business Acumen Strong executive presence with the ability to engage confidently at C‑suite and senior leadership levels. Exceptional business acumen and strategic thinking, with a customer- and market-oriented mindset. Excellent communication skills, both written and verbal. Ability to operate effectively in a complex, global, matrixed organization. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is 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 $125,300.00 - $349,000.00. 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.

Job OverviewPerform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies. Essential Functions• Provide clinical research support to investigators and site staff, including• Verify and/or correct research study information on source documents; research queries and variances; and providefeedback to the site data collector.• Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control for content,accuracy, and completeness.• Prepare and maintain research study files. Compile, collate and submit study information within established deadlines.• Collect and submit regulatory/ethics documentation pertaining to the research study.• Maintain the FDA 1572 form for assigned research studies.• Schedule subject visits and generate appropriate reports and documents for research subjects prior to visits.• Input visit data into clinical trial management system (CTMS) to track patient visits and procedures completed against the study budget. Qualifications• Bachelor´s Degree in Life Sciences or related concluded (required)• 6months to 1 year of experience working at a clinical research site • Conversational Intermediate English • Basic knowledge of clinical trials• In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and studyschedules• Basic knowledge of medical terminology• Basic skill in using MS Windows and Office applications such as Access, Outlook, Excel, and Word• Excellent interpersonal skills• Ability to pay close attention to detail• Ability to establish and maintain effective working relationships with coworkers, managers and clients•  Applicable certifications and licenses as required by the company, country, state, and/or other regulatory bodies Upon Hire 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.

Únete a nosotros en nuestro emocionante trayecto! IQVIA ™ es The Human Data Science Company ™, enfocada en el uso de datos y ciencia para ayudar a los clientes de la salud a encontrar mejores soluciones para sus pacientes. Formada a partir de la fusión de IMS Health y Quintiles, IQVIA ofrece una amplia gama de soluciones que aprovechan los avances en información, tecnología, análisis e ingenio humano para impulsar la atención médica. Actualmente nos encontramos en la búsqueda de profesionales que quieran ser parte de un gran proyecto con una farmacéutica multinacional. Representante de Farmacias Objetivo del cargo Responsable de la educación a los farmaceutas presencial y remota del portafolio del laboratorio, realizar el seguimiento de las existencias de las marcas en las diferentes cadenas de farmacias comerciales e institucionales asignadas a su territorio, asegurando la distribución y el abastecimiento para atender la demanda generada de los productos en cada una de las farmacias Principales Funciones Promocionar productos para la línea asignada en las farmacias de cadena de las de los principales distribuidores (Retail) y operadores logísticos de las Eps para el despacho de medicamentos en lo relacionado a su territorio presencial y remotoConstruir relaciones efectivas con su panel de farmaciasMantener actualizada toda la información de su panel de farmaciasManejar las herramientas para la gestión de su territorioHacer seguimiento de la distribución de sus productos en las farmacias asignadasConocimiento de la enfermedad y del portafolio que promocionaAsegurar las metas de venta y los indicadores establecidos para su territorioAdherirse a los lineamientos de ética en los negociosRequisitos Tecnólogo o estudiante en cursoExperiencia de 1 año en adelante en posiciones similares, preferiblemente con experiencia en visita a farmacias de cadenaManejo de paquete office.Manejo de CRM (deseable)Comunicación empática y asertiva e influencia para crear relaciones con su panel de farmacias, centradas en las necesidades de estas.Competencias de orientación a resultados, planeación, organización y orientación al cliente.Persona comprometida, disciplinada, proactiva, autónoma y organizadaCiudad de residencia: Barranquilla (Disponibilidad de viaje a Valledupar).#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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA™ – 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 88.000 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. Dazu gehören integrierte Projektansätze entlang unseres IQVIA-Lösungsportfolios, die wir individuell an Kundenbedürfnisse anpassen und aus einer Hand anbieten. Für einen bundesweiten Teamaufbau im Bereich Dermatologie suchen wir zum 1. Mai 2026 einen erfahrenen Regional Sales Manager (m/w/d). Gebiet: Nord Rollenbeschreibung: Führung und Weiterentwicklung eines Teams von Key Account Managern Sicherstellung der konsistenten Umsetzung von Launch-Prioritäten Übersetzung der nationalen Strategie in regionale Aktionspläne Etablierung einer starken Leistungs- und Verantwortlichkeitskultur Steuerung der regionalen Ergebnisse anhand von KPIs und Performance-Kennzahlen Identifikation von Risiken und Einleitung geeigneter Gegenmaßnahmen Rolle als Coach auf erster Führungsebene und als Vorbild Sicherstellung eines qualitativ hochwertigen Onboardings sowie kontinuierlicher Weiterentwicklung Enge Zusammenarbeit mit der nationalen Führungsebene und unterstützenden Funktionen Umgang mit Komplexität in Matrix- und Outsourcing-Strukturen Sicherstellung der Einhaltung von Compliance- und Governance-Vorgaben Förderung von Team-Engagement, Motivation und Mitarbeiterbindung Erforderliche Qualifikationen: Hochschulabschluss in den Life Sciences oder in Betriebswirtschaft (gemäß §75 AMG) Mehrjährige Führungserfahrung im pharmazeutischen Vertrieb Fundierte Kenntnisse des deutschen Pharmamarktes sowie der Compliance-Anforderungen Hohe Reisebereitschaft Verhandlungssichere Deutschkenntnisse (C1–C2) Erforderliche Erfahrung: Führung von Außendienstteams, idealerweise in Launch- oder Transformationsphasen Erfahrung im Performance Management sowie in KPI-basierter Steuerung Erfahrung in Rekrutierung, Onboarding und Talententwicklung Erfahrung in der bereichsübergreifenden Zusammenarbeit Erfahrung mit hybriden oder ausgelagerten Modellen (von Vorteil) Zentrale Fähigkeiten & Kompetenzen: Starke, positive und lösungsorientierte Führungspersönlichkeit mit hoher intrinsischer Motivation, die Teams zu ambitionierten Zielen inspiriert Ausgeprägtes Führungs- und Coaching-Mindset zur Förderung kontinuierlicher Entwicklung und hoher Leistungsfähigkeit Hervorragende kommunikative Fähigkeiten auf Führungsebene – klar, überzeugend und verlässlich auf allen Stakeholder-Ebenen Strategischer Kundenfokus mit ausgeprägter Account-Ownership-Mentalität, um Erkenntnisse in nachhaltigen Geschäftswert zu übersetzen Proaktive, zukunftsorientierte Führungskraft mit hohem Verantwortungsbewusstsein, die Entscheidungen und Ergebnisse konsequent vorantreibt Hohe Umsetzungsstärke und Resilienz, auch in dynamischen oder herausfordernden Situationen Ausgeprägte Umsetzungsdisziplin zur Sicherstellung operativer Exzellenz, Konsistenz und Zuverlässigkeit Strategisches und operatives Denken mit der Fähigkeit, langfristige Visionen und tägliche Effektivität in Einklang zu bringen Analytische und erkenntnisbasierte Entscheidungsfindung mit ausgeprägter Dateninterpretationskompetenz Hohe Analyse- und Entscheidungskompetenz zur sicheren Urteilsbildung in komplexen Umfeldern Nachgewiesene Führungserfahrung in bereichsübergreifenden Strukturen mit Fokus auf Alignment und starke Zusammenarbeit Inklusiver und befähigender Führungsstil im Umgang mit diversen Teams und komplexen Stakeholder-Landschaften Fähigkeit, Teams durch Veränderungsprozesse zu führen und dabei Klarheit, Stabilität und Orientierung zu geben Affinität zu Multichannel-Vertrieb und modernen digitalen Interaktionsformaten sowie sicherer Umgang mit digitalen Tools zur Steigerung von Kundenerlebnis und Teamperformance 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 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  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 #PharmaceuticalSales #RSM #Leadership #Pharmacy #FieldSales #Dermatology 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.

About the Role We are looking for a Supplier Services Coordinator to join our dynamic team. In this role, you will play a key part in managing relationships with data suppliers, ensuring high-quality data collection, and supporting our clients across the pharmaceutical ecosystem. This is an excellent opportunity for someone who enjoys working with data, building relationships, and contributing to meaningful projects in the healthcare industry. Key Responsibilities Build, manage, and grow relationships with data suppliers across assigned panels Recruit and onboard new suppliers, ensuring strong engagement in IQVIA programs Ensure timely, accurate, and consistent data collection (both electronic and manual) Monitor data quality, identify issues, and collaborate with internal teams to resolve them Manage supplier compensation and incentive processes Provide responsive support to clients, including pharmaceutical companies Participate in client meetings and contribute to ad-hoc analyses and special projects Maintain accurate supplier records and panel data Deliver training and guidance on IQVIA tools and reporting solutions Key requirements Experience At least 2 years of experience within the pharmaceutical industry (e.g., wholesalers, pharmacy chains, or similar environments) Education & Knowledge University degree or equivalent Basic understanding of systems, processes, and data handling Good Excel knowledge at intermediate level Experience with IQVIA products is a plus Fluency in English and local language Skills Strong analytical and problem-solving abilities Excellent communication and relationship management skills Ability to manage multiple priorities and work effectively under pressure Customer-focused mindset with strong account management capabilities Proactive approach to identifying issues and driving solutions High level of professionalism, ownership, and initiative Why Join IQVIA? Be part of a global organization making a real impact on healthcare Collaborate with diverse, talented teams across multiple markets Gain exposure to leading pharmaceutical clients and data-driven solutions Enjoy opportunities for growth, learning, and career development IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

We are seeking a highly skilled Senior Generative AI Engineer to join our pioneering team. In this role, you will be instrumental in developing the Orion platform, focused on accelerating the development and delivery of GenAI products. You will help standardize and simplify our technology stack, provide essential components to foster innovation, and shield application teams from technical complexities, enabling them to focus on what they do best.  Key Responsibilities Platform Development:  Design and architect the Orion GenAI Platform to support scalable and efficient GenAI product deployment.  Accelerate Development:  Implement strategies to speed up the development and delivery lifecycle of GenAI products.  Standardization:  Develop and enforce standardized technology stacks and best practices to ensure consistency and quality across projects.  Innovation Facilitation:  Provide standard components and tools that enable application teams to innovate rapidly without reinventing the wheel.  Technical Shielding:  Abstract and manage complex technical challenges, allowing application teams to focus on application-specific functionalities.  Collaboration:  Work closely with cross-functional teams to understand their needs and integrate GenAI solutions seamlessly. Qualifications Software Design & Architecture:  Proven experience in designing robust software architectures for large-scale platforms.  Development Best Practices:  Strong understanding of software development and delivery best practices, including CI/CD pipelines, version control, and testing methodologies.  Generative AI Expertise:  Deep knowledge of transformer architectures, embedding models, large language models (LLMs), Retrieval-Augmented Generation (RAG), and AI agents.  Data & ML Engineering:  Solid background in data engineering and machine learning engineering. Experience with  Databricks  is a plus.  Cloud Proficiency:  Extensive experience with cloud platforms, preferably  Azure .  Advanced Python:  Expertise in advanced Python programming for developing complex AI models and applications.  Web Technologies:  Proficiency in web development technologies, particularly  JavaScript , for building interactive and user-friendly interfaces.  Performance Optimization:  Experience with parallel processing and GPU/CUDA programming is a nice-to-have.  Master's Degree in Machine Learning, Statistics, Computer Science, Physics, Math, or related field is preferred. at least 8 years of software engineering experience, relevant experience with AI with a focus on GenAI. 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.

Role & Responsibilities The IQVIA Patient Centered Solutions group has an opportunity for a Manager to join the team to support Licensing & Distribution activities. In this role you will be responsible for managing the licensing and electronic implementation processes of Clinical Outcome Assessments (COAs) to be used in Clinical Trials, serving as primary contact with external vendors and internal departments. Also accountable for tracking the performance of assigned COAs businesses, including sales/revenue and staff allocation. Specifically, your role will include: Oversight and management of the operational aspects of COA licensing activities and programs from study initiation through to closeout including partnering with study project managers, setting up of vendors within IQVIA systems, facilitating legal reviews/approvals, and ultimately ensuring quality deliverables are on time and within budget. Creating, tracking and reporting on COA licensing project support timelines. Financial reporting on the COA licensing projects including tracking deliverables and invoicing. Monitoring, managing, and communicating expectations and activities related to COA licensing to cross-functional project teams. Coordinating with other project resources within and outside the organization. Negotiating COA licensing costs and contracts. Developing and maintaining internal databases of COA licensing requests and project plans. Participating in proposal development and sales/proposal presentations for COA licensing. Meet with team members on a regular basis regarding project tasks to ensure project milestones are met. Ensure that work is conducted in compliance with standard processes, policies and procedures and meets project timeline metrics. REQUIRED KNOWLEDGE, SKILLS AND ABILITIES Bachelor's degree or equivalent in life sciences, other sciences, or related disciplines. 4+ years’ work experience in clinical research, medical affairs, vendor management, or other related scientific roles. 2+ years’ work experience in a Project Management, Consulting, or other similar client facing role. Solid understanding of the pharmaceutical industry and drug development process. Fluency in English (spoken and written). Excellent communication, presentation and interpersonal skills including the ability to communicate effectively with both technical and non-technical audiences. Results and detail-oriented approach to work delivery and output and excellent problem-solving skills. Excellent planning, time management and prioritization skills. Demonstrated ability to deliver results to the appropriate quality and timeline metrics. Ability to think and develop initiatives independently in alignment with the expectations of usual Project Management approaches. Sound judgement and ability to establish and maintain effective working relationships with coworkers, managers, and clients. Strong software and computer skills, including MS Office applications. Familiarity with IQVIA business units / functions and ability to navigate the organization effectively is a plus 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.

Profile Overview Senior Business Analyst – Healthcare Information Systems is a critical client-facing role focused on the analysis and implementation of healthcare IT solutions. This position leverages a strong clinical background and in-depth understanding of local and EU healthcare regulatory requirements to guide business requirement studies, ensure compliance, and deliver effective systems tailored to clinical and administrative needs. Key Responsibilities · Lead comprehensive business requirement studies with healthcare clients, ensuring all stakeholder needs are understood and documented. · Engage directly with clients, including clinical and administrative teams, to facilitate requirements gathering and solution design. · Ensure all systems and processes comply with relevant local and EU healthcare regulations, including data protection and clinical safety standards. · Analyze existing healthcare information systems and identify opportunities for improvement, optimization, or regulatory alignment. · Prepare clear documentation of business requirements, process flows, and regulatory considerations for both technical and non-technical audiences. · Collaborate with IT, compliance, and clinical teams to translate business needs into actionable system specifications. · Support project delivery, including user acceptance testing and post-implementation review, to confirm solutions meet business and regulatory requirements. · Assist project manager on project planning and scheduling. Required Qualifications · Demonstrated experience working with healthcare information systems in a hospital, clinical, or public health environment. · Good knowledge of local and EU healthcare regulatory frameworks (e.g., GDPR, MDR, local health authority requirements). · Proven ability to lead business analysis activities with multidisciplinary teams and external clients. Skills and Competencies · Strong analytical skills for interpreting complex clinical workflows and regulatory requirements. · Exceptional communication abilities, both verbal and written, to interact with diverse stakeholders. · Demonstrated leadership in facilitating workshops, meetings, and requirement-gathering sessions. · Expertise in healthcare regulatory compliance, including data privacy, patient safety, and clinical governance. · Proficiency in documentation, process mapping, and business analysis tools. · Ability to manage multiple projects and priorities in a dynamic healthcare setting. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewUnder broad guidance, ensures clients obtain maximum value from products and services in order to facilitate a positive and productive long-term relationship, either broad client or offering focused.Essential Functions• Ensures fulfillment of contract specifications and ad-hoc client requests to build client satisfaction, under supervision.• Assists team members to build, establish and maintain effective business relationships with clients to proactively support their needs as their day-to-day contact, possibly focused on a specific product or service.• Ensures, through review and verification, that the product deliverable meets the customer's specifications, including timeliness and quality.• Partners with the account manager and clients to derive optimum value from IQVIA products and services by explaining and expanding the usage of current IQVIA deliverables and identifying revenue opportunities within existing clients.• Maintains effective internal communications with sales and client service support to keep all apprised on activities with the client.• Monitors performance against existing service agreements and ensures client’s obligations are met.• Researches, analyzes and responds to client that require an in-depth understanding of the client, specific business line, and/or therapeutic market.• May conduct product/services and process training for clients and other employees.• May conduct service meetings at client sites.• Represents IQVIA on external client projects.• May mentor and lead other client service reps and represent the manager in their absence.Qualifications• Bachelor's Degree Req• 5-7 years of related work experience Req• Broad knowledge of the concepts, practices and procedures of the client service representative field Req• Broad knowledge of IQVIA products and the Pharmaceutical industry Req• Meeting facilitation, presentation and training experience Req• Proficiency in PC applications, such as Excel• Ability to communicate effectively with various levels in the organization (written and oral) and to manipulate large transactional databases• Demonstrated problem solving, analytical and strong customer service skills• Demonstrated ability to develop and maintain relationships in a diverse business environment• Ability to travel to clients and IQVIA offices as appropriate•Accreditation preferred in multiple business lines of IMS service certification program Req   Shift: 6:30 PM to 3:30 AM ISTIndia holidays working/US holidays off 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 Title: Registered Dietician - IndianaLocation: Remote in United States Job Type: Per Diem IQVIA are looking for experienced Dieticians to join our team. The ideal candidate will have experience in providing dietary advice and support to individuals with rare diseases. Key Responsibilities: Our remote Registered Dieticians are responsible for: Conduct nutritional assessments and develop personalized dietetic plans for clients with various disease classifications via telecommunications. Provide ongoing dietetic counselling and support to clients and their familiesNutritional assessments and dietetic counseling (only done for clients in which you are licensed to practice.) Maintain accurate and confidential client recordsParticipate in virtual team meetings and training sessionsQualifications:Qualified Registered Dietician (CDR) with Current National Registration and in-state licensure (except CA, MI, NJ, AZ, VA, and CO)In-state licensure: Unencumbered and active state license requiredMulti-state license in NY, FL, and TX preferredMinimum 1 year of experience planning for and coaching patientsMinimum 1 year of experience working remotely via telehealthExcellent communication and interpersonal skillsExperience working with patients with obesity (with and without diabetes) preferredExperience managing patients on GLP-1 preferredBilingual (Spanish/English) requiredNote: This position is not eligible for sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote 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 45 per hour. 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.