IQVIA

AI Technical Product Manager Location: Poland, Greece, Czech Republic, Italy, Spain, Portugal, home-based Role Description We are seeking an AI Technical Product Manager/Product Owner to own Agentic AI products across Proof of Concept, MVP, and Production. This role is responsible for translating product intent and business needs into clear, testable, agent‑ready requirements, and for ensuring that autonomous and semi‑autonomous agents deliver the expected outcomes in real‑world, regulated environments. Operating as part of the ATS CAITI Core Development Team, the AI Product Owner owns the product backlog, acceptance criteria, and Definition of Ready, and acts as the primary execution‑time liaison between Product, Engineering, Architecture, QA/Validation, and Business. The role works closely with the AI Product Manager to support scope and prioritization decisions, while maintaining day‑to‑day ownership of product execution. Key Responsibilities Own the execution‑level product ownership of Agentic AI solutions across Proof of Concept, MVP, and Production.Translate business needs and product intent into agent‑ready user stories, workflows, and acceptance criteria.Own and maintain the Agentic AI product backlog, ensuring clarity, readiness, and alignment with delivery constraints.Define and enforce Definition of Ready and acceptance standards suitable for autonomous and human‑in‑the‑loop agent workflows.Drive backlog prioritization and refinement, balancing agent capabilities, evaluation readiness, non‑functional requirements, and delivery feasibility.Partner with AI Product Managers to support MVP scope and sequencing decisions, ensuring feasibility and readiness against value hypotheses and success KPIs.Collaborate closely with Architecture, Engineering, and UX to shape agent behavior, orchestration patterns, guardrails, and exception handling early in the lifecycle.Act as the primary execution‑time product contact for engineering teams, clarifying intent, resolving scope questions, and validating delivered outcomes.Own story acceptance and UAT, ensuring delivered agent behavior meets defined success criteria, quality expectations, and regulatory requirements.Manage the post‑release backlog for enhancements, defects, and agent tuning, informed by telemetry, user feedback, and operational insights.Key Qualifications Experience 4–6+ years as a Product Owner, Technical Product Manager, or similar role delivering Agentic AI, AI, data, or workflow‑driven products.Hands‑on experience owning backlogs and requirements across PoC, MVP, and Production lifecycles.Proven ability to work effectively with cross‑functional teams and deliver high‑quality software solutions.Agentic & Technical Background Bachelor’s degree in a STEM field (Computer Science, Engineering, Data Science, Information Systems, Mathematics, or related discipline), or equivalent practical experience spanning product management, software delivery, and AI/data systems.Experience translating requirements for AI or Agentic systems, including workflows involving reasoning, orchestration, and human‑in‑the‑loop patterns.Solid understanding of software architecture fundamentals, APIs, data flows, and agile delivery practices.Ability to reason about agent behavior, failure modes, and acceptance criteria, even without being the technical implementer.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 155 600,00 zł - 289 200,00 zł. 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 Family Description Conducts statistical analyses for client reports and publications, performs advanced statistical programming and biostatistical analyses and utilizes findings, and insights for practical application to further business operations, come across innovative findings and discoveries for solution and product development. Sub-Family Description • In an FSP environment, the subject matter expert develops, executes, and reviews programs to provide statistical programming support for clients to source, organize (creating statistical tables, listings, and graphs) and interpret complex data sets. • Creates programming specifications, program development, program validation, and program output finalization associated with analysis datasets, tables, figures, listings, and regulatory submission data packages; and provides programming support for additional business needs such as safety reporting, patient data reviews, and risk mitigation. • Resources are assigned full time to a client and utilize customer SOPs, training, and protocols 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.

Make a Difference with IQVIA Australia – Join Our Nursing TeamAre you a nurse looking for flexibility and the chance to make a real impact? At IQVIA, we empower nurses across Australia to deliver high-quality care in patients’ homes—changing lives, one visit at a time. As a Casual Registered Nurse, you’ll provide essential care outside the hospital setting, traveling to patients’ homes to deliver treatments with precision and compassion. What You’ll Be Doing IV cannulationSubcutaneous and intramuscular injectionsPossible blood sample collectionECGs, vital signs, and observationsWhat’s in It for You? Competitive hourly payFlexible work arrangementsSupportive, inclusive environmentValuable community nursing experienceWho We’re Looking For Whether you’re early in your nursing career or highly experienced, we welcome your skills and passion. You’ll need: Current AHPRA registration (Registered Nurse)Experience with IV cannulation, subcutaneous, and intramuscular injectionsCurrent CPR certificationStrong patient-centered care ethosExcellent communication and interpersonal skillsAvailability during business hours, Monday to FridayWhy IQVIA? With multiple roles available, we offer opportunities that fit your lifestyle and professional goals. At IQVIA, your work supports real people, real progress, and real change in healthcare. Ready to make a difference? Apply now and join a team that’s redefining healthcare—one patient at a time. 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™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen. Werden Sie Teil unserer Community von rund 86.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welche Rolle Sie bei IQVIA einsteigen, es erwartet Sie ein offenes, innovationsfreudiges Umfeld, in dem Sie sich viel bewegen können. Finden Sie heraus, wie Sie Ihre Talente und Ihre Leidenschaften bei IQVIA einbringen können. Im Bereich Commercial Engagement Services (CES) arbeiten wir eng mit unseren Life Sciences-Kunden zusammen und unterstützen sie mit flexiblen Vertriebs- und Personallösungen für nachhaltigen Erfolg am Markt. Dies umfasst insbesondere die Rekrutierung, das Training und die Steuerung des Vertriebsteams in Dienstleistungsprojekten bzw. in Arbeitnehmerüberlassung. Dabei differenzieren wir uns über integrierte Projektansätze entlang des IQVIA Lösungsportfolios, die wir individuell an die Kundenbedürfnisse anpassen und aus einer Hand anbieten. Komm in unser IQVIA-Team!Für ein spannendes Projekt im Bereich Hämatologie suchen wir Pharmaberater (m/w/d) zum nächstmöglichen Zeitpunkt Im Gebiet: Würzburg, Nürnberg, Regensburg Das sind Deine Aufgaben: Identifizierung und Zuordnung der wichtigsten Accounts, Kunden und Entscheidungsträger in diesen Accounts aus dem Bereich der Hämatologie und Erstellung eines maßgeschneiderten Plans für jeden Account. Empfehlen und Entwickeln von maßgeschneiderten Lösungen für seinen Kunden und die Account-Netzwerke, denen der Kunde angehört. Durchführung von kompetenten Fachgesprächen nach VBS (Wertorientiertes Verkaufen) in den Fachgruppen der Hämato-Onkologen sowie Betreuung von ausgewählten onkologischen Pflegekräften. Umsetzung der Vertriebs- und Marketingstrategien der Geschäftseinheit. Dazu gehören der Außendienst und die Durchführung von Veranstaltungen, wie z.B. das Sponsoring der wichtigsten lokalen Veranstaltungen und Peer-to-Peer-Meetings. Erstellung und kontinuierliche Weiterentwicklung strategischer Analysen der betreuten Kunden (inkl. SWOT-Analyse, Patientenströme, Volumen dieser potenziellen Kunden) und Umsetzung der auf diesen Analysen basierenden Empfehlungen.  Aufbauend auf den bestehenden und Entwicklung neuer Zugangswege zu wichtigen Entscheidungsträgern, einschließlich persönlicher und virtueller Besuche für alle Kunden, unter Anwendung eines kundenspezifischen Multi-Channel-Ansatzes. Förderung und Umsetzung von Kontaktwegen für jeden Kunden, um eine optimale Frequenz über die vom Kunden bevorzugten Kanäle zu erreichen. Das bringst Du mit: Ausbildung zum geprüften Pharmareferenten oder wissenschaftliche Ausbildung (idealerweise Hochschulabschluss). 3-5 Jahre Berufserfahrung als erfolgreicher Pharmareferent/in in der Hämato-Onkologie. Die Fähigkeit und das Wissen, onkologische Kunden in gesundheitspolitischen Fragen zu beraten. Erfahrungen und Erfolge mit "Value Based Selling". Ein klares Verständnis von wertorientiertem Verkaufen und ausgezeichnete Verkaufsfähigkeiten in diesem Bereich. Bereitschaft, neue Zugangsmöglichkeiten über mehrere Kanäle zu entwickeln und umzusetzen. Hervorragende Zusammenarbeit und nachgewiesene Fähigkeit, mit unterschiedlichen Teams Ergebnisse zu erzielen. Hohe Lernflexibilität und Lösungsorientierung. Teamfähigkeit (Wir > ich). Ausgeprägtes strategisches, analytisches und kreatives Denken. Nachgewiesene Fähigkeiten zur Eigenverantwortung. Technische Affinität Das erwartet Dich bei uns: Ein attraktives Gehaltspaket plus Kundenprämien, vielfältige Corporate Benefits, betriebliche Altersvorsorge sowie 24/7 Unfallversicherung (auch für den privaten Bereich) und exklusive private Krankenzusatzversicherungen Ein top ausgestatteter Firmenwagen verschiedener Premiumanbieter mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des Modells  Eine moderne IT-Ausstattung für Deinen modernen digitalen Arbeitsplatz Unser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige Perspektive Wir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines Wohnorts  Eine hohe Übernahmequote durch unsere Kunden ermöglicht Dir den Karrierestart bei zukunftsweisenden und führenden Unternehmen der Pharmabranche und Medizintechnik-Branche Vielfältige und individuelle Weiterentwicklungsmöglichkeiten auch innerhalb von IQVIA (z.B. Führung, Key Account Management, Projektmanagement und vieles mehr) Wir begleiten Dich während Deiner Bewerbungsphase durch individuelle Betreuung/Vorbereitung bis zur Einstellung und auch darüber hinaus während des Beschäftigungsverhältnisses Unser Kunden-Netzwerk reicht vom Start-up Unternehmen bis zum Global Player. Gemeinsam mit Dir finden wir den richtigen Job für Dich! Starte Deine Karriere mit IQVIA! Dein besonders schneller Draht zu uns: Kandidaten-Hotline: 0621-84508113 oder sende uns gerne direkt Deine Bewerbung per Mail an: [email protected]  #LI-CES #LI-DNP #LI-SS2 #Pharmaberater #Biologie #Chemie #Pharmareferent #BTA #CTA #PTA #Onkologie #Hämatologie #Facharzt #Pharmazie #Pharma-Außendienst IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. Bei IQVIA Contract Sales & Medical Solutions unterstützen Sie unsere Kunden darin, dem Gesundheitswesen neue Impulse zu geben. IQVIA hat die weltgrößte "Commercial Solution Organisation" die es ermöglicht, den Markteintritt und das Marketing von Produkten länderspezifisch, regional oder global mit rund 10.000 Mitarbeitern im Außendienst in mehr als 30 Ländern durch die Ansprache von Ärzten und Patienten zu optimieren. 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. Dies umfasst insbesondere die Rekrutierung, das Training und die Steuerung des Vertriebsteams in Dienstleistungsprojekten bzw. in Arbeitnehmerüberlassung. Dabei differenzieren wir uns über integrierte Projektansätze entlang des IQVIA Lösungsportfolios, die wir individuell an die Kundenbedürfnisse anpassen und aus einer Hand anbieten. Für ein globales Unternehmen, das sich für die Verbesserung der Gesundheit und der Lebensqualität von Menschen mit Diabetes einsetzt, suchen wir zum nächstmöglichen Zeitpunkt erfahrene Medizinprodukteberater (m/w/d) mit Status nach § 75 AMG. Ihr Gebiet: Stuttgart, Ludwigsburg, Schwäbisch-Hall, Kempten Das sind Ihre Aufgaben: Betreuung von diabetologischen Schwerpunktpraxen, Kliniken, API und Apotheken Umsetzung der Marketing- und Vertriebsstrategien, Produktschulungen sowie Unterstützung bei Fragen und Problemen Selbstmonitoring und Anpassung der Maßnahmen an die aktuelle Marktsituation nach Rücksprache mit dem Regionalmanager Umsetzung der Preisstrategie im Klinikgeschäft Selbstständige, zielorientierte Planung, Durchführung und divisionsspezifische Nachbearbeitung von Kundenbesuchen Organisation und Durchführung von Kodex- und Compliance konformen Schulungs- und Fortbildungsmaßnahmen bei der Zielgruppe Strategisches Account Management, Identifizierung und Nutzung von Netzwerken Hilfestellung bei gesundheitspolitischen Fragestellungen in Abstimmung mit dem Key Account Manager Beobachtung der Markttrends/Wettbewerber  Einhaltung der gesetzlichen Vorschriften nach MPG, HWG und UWG sowie aller relevanten Verhaltenskodizes.  Teilnahme an Kongressen und Fortbildungsveranstaltungen Reporting auf Basis des ADC-eigenen Systems  Das bringen Sie mit: Abgeschlossene kaufmännische oder naturwissenschaftlich angelehnte Ausbildung Sachkenntnisse als Pharmaberater (m/w/d) gem. § 75 AMG Mehrjährige Außendiensterfahrung sowie ein ausgeprägtes verkäuferisches Geschick Vertriebs-, kunden- und marketingorientierte Denkweise Sicheres Auftreten und Beharrlichkeit Hohe Eigeninitiative und Selbstmotivation Freude am Aufbau und an der Pflege von vielfältigen Kontakten Fachkenntnisse in der Indikation Diabetes wünschenswert Kompetenzen: Persönliche Entwicklungsfähigkeit, Kundenorientierung, Ergebnisorientierung, Entscheidungsfähigkeit, Bewältigung von Komplexität Gute kommunikative Fähigkeiten Erfolgswillen Identifikation mit dem Berufsbild Teamfähigkeit und hohe soziale Kompetenz Eigenmotivation und Erfolgswillen Kontaktfreudigkeit Kritikfähigkeit und Wille zur Weiterentwicklung  Zuverlässigkeit und Flexibilität Positive Ausstrahlung Gute EDV-Kenntnisse Tätigkeiten der Außendienstmitarbeiter (m/w) Das bieten wir Ihnen: Ein attraktives Gehaltspaket Vielfältiger Fahrzeugpool verschiedener Premiumanbieter auch zur Privatnutzung (ohne Zuzahlung)  Moderne IT-Ausstattung  Umfangreiche Sozialleistungen Projektbezogene Prämiensysteme Sicherheit (unbefristete Arbeitsverträge) Vielfältige und individuelle Weiterentwicklungsmöglichkeiten  Abwechslungsreiche Projektvielfalt in verschiedenen Indikationen Unsere zusätzliche Dienstleistung für Sie: Mit Ihrer Bewerbung eröffnen Sie sich Zutritt zu unserem gesamten Kundennetzwerk. Wir berücksichtigen Ihre Bewerbung nicht nur für diese Position, sondern für alle aktuellen und zukünftigen Positionen in unserem Hause und bei unseren Kunden.  #LI-CES #LI-DNP #LI-SS2 #Pharmaberater #Medizinprodukte #Diabetes #Facharztaußendienst #Pharmareferent 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 Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring in oncology. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. Job OverviewWe are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials. In this position, you will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. Your work will directly contribute to the integrity and quality of clinical research data. Key Responsibilities Conduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines. Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals. Deliver protocol and study-specific training to site personnel and maintain consistent communication to manage expectations and resolve issues. Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity. Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries. Ensure that essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File (ISF) in accordance with regulatory standards. Document site management activities, visit outcomes, and follow-up actions through detailed reports and correspondence. Work closely with cross-functional project teams to support study execution and ensure alignment with project goals. Depending on the project, you may also support site-level recruitment planning and financial management, including invoice collection and budget tracking. Qualifications Bachelor’s degree in life sciences or health-related field (or equivalent experience). Requires at least 1 year of on-site monitoring experience. Strong understanding of GCP, ICH guidelines, and regulatory requirements. Ability to travel as required by the project. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

To be eligible for this position, you must reside in the same country where the job is located. This role is hybrid and will require going into an IQVIA office several times weekly in PA, NY, NJ or CT.Consultant - Commercial Solutions & Insights Hub (CSIH), Analytic ServicesIQVIA CSIH is a market-leading, service delivery-oriented division within IQVIA Commercial Solutions. CSIH team members consult with manufacturers in the pharmaceutical and biotechnology industries to meet the challenges of today’s complex and evolving healthcare landscape. Analytic Services leverages the power of healthcare data to help its clients formulate methodologies that answer business questions in a broad spectrum of areas of expertise-providing deep insights into patient, payer, and prescriber behaviors. As a valued member of the Analytic Services team, you will actively: Design analytics and execute them. You will acquire knowledge of IQVIA data sources, lead analysis to inform strategic recommendations, develop data analyses systems, and identify trends in complex data sets.Provide business consulting and project management: You will apply consulting methodologies to deliver engagements, create presentations for clients, manage projects, cultivate professional relationships with client teams, and work with management to prioritize needs.Synthesize complex data into actionable results and recommendations from the evaluation of secondary data sources to answer a wide range of market, therapeutic, prescriber, patient, payer, and competitive related questions.Assist in developing detailed documentation and specifications, including business process documentation, SOPs, and client data scorecards.CSIH seeks team members who demonstrate strength in our core competencies including: OwnershipGrowthInnovationCollaborationAs a member of the team, you will have the opportunity to not only learn from but also contribute to the vibrant CSIH community. You will participate in learning communities to codify your data analytics subject-matter expertise and develop training content available to the entire team. Required Skills & Experience: Bachelors degree or higher education required.3-5 years of related experience including consulting and life sciences industry experience.Strong ability to manage priorities to meet deadlines with consistent, high-quality outcomes.Knowledge of the fundamental processes of pharmaceutical commercial business.Prior healthcare data experience, including working knowledge of physician and patient claims; IQVIA data preferred.Prior working experience in marketing analytics including patient journey, segmentation, targeting, promotion, allocation, sales force sizing and optimization, ROI, Tracking: Utilization, SOB, LOT, Etc.; forecasting and launch, model building, patient analytics, ad-hoc and tracking of LAAD and patient data; supply/supply chain analytics, access: co-pay, performance, customer profiling, reversal/rejection analysis, adherence curves.Demonstrated knowledge in MS Excel, MS Access, and MS PowerPoint.Experience in data visualization software including Power BI and Tableau.Strong technical skills in any of the following: SAS, SQL, R, Python, and/or Excel VBA.Exposure to cloud processing environments such as Cloudera, Snowflake, and/or Databricks.Experienced with developing consultative relationships with senior level managers and executives at clients in the life sciences industry.Knowledge of consulting methodologies, tools, and techniques related to functional area.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 $68,300.00 - $170,000.00. 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.

Plan and conduct independent clinical (GCP) audits to assess compliance with regulations, guidelines, and operating procedures. Prepare and distribute reports of findings to supervisor, operations staff, management, and customers. Provide consultation in interpretation ofregulations, guidelines, policies, and procedures. Support management in promotion and assessment of compliance to regulations, guidelines and corporate policies. Essential Functions• Plan, schedule, conduct, report and close audit activities in any of the countries involved with IQVIA contracts to assess compliance with applicable regulations/guidelines, customer requirements, IQVIA SOPs and project specific guidelines/instructions• Evaluate audit findings and prepare and distribute reports to operations staff, management, and customers• Provide interpretation and consultation to project teams on regulations, guidelines, compliance status, and policies and procedures• Provide consultation to customers and monitors in interpretation of audit observations and formulation of corrective action plans• Review, approve investigations, Root Cause Analysis (RCA), Corrective Action Prevention (CAPA) and Effectiveness Check (EC) plans and track till closure for quality events arising from Audits; and from Quality Issues, Inspections or during similar QA activities as assigned.• Evaluate policies and procedures for compliance with applicable regulations/guidelines and provide recommendations to management for continuous process improvements• Maintains the electronic quality management system (eQMS) and provides support in relation to the audit lifecycle• Lead/collaborate/support in QA initiatives/projects for quality, process improvements• Assist in training of new Quality Assurance staff• May be required to manage Quality Issues• May present educational programs and provide guidance to operational staff on compliance procedures• May perform pre-inspection visits at sites, host audits/inspections; ensure proper conduct of customer-initiated audits and mock regulatory inspections, and assist in regulatory facility inspections, as assigned. Qualifications• The right candidate must be Certified to conduct audits in Italy in accordance with the Italian Decree of the Ministry of Health dated 15 Nov 2011. • Travel 30-50% mainly in Europe.• 5 years experience in pharmaceutical, technical, or related area, of which 3 years in Quality Assurance Audits.• Experienced in the conduct of clinical trial Investigator site audits.• Experience in the conduct of clinical study report/data management clinical trial audits is preferred.• Knowledge of word-processing, spreadsheet, and database applications.• Extensive knowledge of pharmaceutical research and development processes and regulatory environments.• Knowledge of quality assurance processes and procedures.• Strong interpersonal skills.• Excellent problem solving, risk analysis and negotiation skills.• Strong training capabilities.• Effective organization, communication, and team orientation skills.• Ability to initiate assigned tasks and to work independently.• Ability to manage multiple projects.• Ability to establish and maintain effective working relationships with coworkers, managers and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is € 47.500,00 - € 71.300,00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Research Nurse – Clinical Trials (Mental Health/Substance Addiction Required)Location: Opportunities at West London and South London sites30 hours per week | 1 year contract | Start: June 2026 IQVIA is hiring an experienced Clinical Research Nurse to support an opioid use disorder clinical trial in London. ⚠️ Important: This role is ONLY suitable for candidates with prior experience in mental health, addiction, or substance misuse. Applications without this experience will not be considered. What you’ll be doing:Supporting patient screening, recruitment, and informed consentCollecting medical history and performing clinical assessments (vitals, ECGs)Managing Investigational Product (IP)Handling lab samples and clinical data entry (EDC, eCOA, CRFs)Supporting AE/SAE reporting and maintaining site documentationCoordinating patient visits and providing ongoing supportWhat we’re looking for:Registered Nurse (active registration)Essential: Proven experience in mental health, addiction, or substance misuse settingsMinimum 2 years’ Clinical Research Nurse experienceStrong clinical trial knowledge and hands-on skills (IP, ECGs, labs)Excellent organisation, communication, and attention to detailWhy IQVIA?Work with a global leader in clinical research on impactful studies in a supportive, professional environment. Apply now if you meet the essential experience criteria and are ready to make a difference in this space. #LI-HCPN #LI-CES #LI-DNP #LI-NS1 #LI-Onsite IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Care Educator / Certified Medical Assistant(Hybrid Role) - Durham, NCPatients are at the center of our business strategies. Care Educator - Patient Engagement Center Program is an educational-based program designed as a resource for patients living with chronic diseases that have been prescribed for specific medications. The Care Educator provides patient-focused education to assist patients to better manage their disease state and access appropriate resources associated with their prescribed medication. Care Educators are responsible for participating in one-on-one communications with patients. The Care Educator interacts with enrolled patients by telephone, video platforms, email, and SMS (text) strictly following the guidelines of the program. The Care Educator program is educational based. Care Educators do not provide medical advice or work clinically within this role. Job Responsibilities:Coordinate and facilitate the connection between patients and program approved, patient-based resources.Provide educational training to patients on specific disease states and medication administration as prescribed by their Healthcare professional.Provide education to foster appropriate dialogue between patients and health care providers.Support treatment decisions made between the patient and healthcare provider.Provide product-related training as outlined in the program guidelines.Help patients build treatment routines and understand and manage side effects.Provide virtual education & support, explaining the treatment journey and guiding the patient through access and financial barriers.Any additional duties assigned by program management.Reinforce behavior change, address concerns, build resilience, and empower patients to stay on therapy long term as prescribed by their HCP.Support long term adherence motivation and QoL goals.ScheduleThis hybrid position will take place primarily in an office setting in the Raleigh area, NC.Able to work a defined shift (8am – 5pm, 9:30am – 6:30pm, 11am – 8pm), with occasional flexibility to support coverage needs across other shifts when required.Flexibility to support patients on Mountain or Pacific time zones as assigned.Must be flexible to work weekends or evenings as needed.Travel 20-40%Required Qualifications:Certified Medical Assistant or equivalent national MA certification (CMA, CCMA, RMA, NCMA, or AMCA).Minimum 3+ years of healthcare experience (e.g., physician’s office, clinic, or specialty care).Skilled at educating or supporting patients in a healthcare setting.Direct interaction with patients and support for persistence and compliance.Knowledge of clinical data and pharmacology.Demonstrated time management skills; planning and prioritization skills; ability to multi-task and maintain prioritization of key projects and deadlines.Demonstrated effective presentation skills; ability to motivate others; excellent interpersonal (written and verbal) skills with demonstrated effectiveness to work cross functional and independently.Demonstrated ability to work and drive results and with enthusiasm.Demonstrated ability to develop and execute plans in an independent environment.Demonstrated ability to take initiative and vision, challenge existing assumptions and interpretations.Demonstrated ability to effectively build relationships with third parties using good negotiation skills.Demonstrated ability to adapt to changing work environments and responsibilities.Fully competent in MS Office (Word, Excel, PowerPoint) and iPad technologyPreferred Qualifications:Previous experience in digestive health and/or gastroenterology preferred.Prior experience working in a virtual or call center environment and providing patient education telephonically preferred.Effective communication and documentation abilities; bilingual (English/Spanish) preferred.Note: This role is not eligible for visa sponsorship. Candidates must have authorization to work in the US without the need for sponsorship. #LI-CES #LI-DNP IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is 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 $50,000 - $55,000 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 Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. IQVIA Biotech is seeking an experienced Clinical Project Manager based in Argentina to lead and deliver innovative clinical trials in Immuno-oncology and Cell and Gene Therapy. As a Project Lead, you’ll drive operational excellence, manage cross-functional teams, and ensure high-quality delivery that accelerates life-changing therapies to market. Key Responsibilities: Lead global/regional clinical trials from start-up through close-out. Develop and execute study management plans aligned with contract and strategy. Manage timelines, budgets, and risk mitigation across projects. Serve as the primary contact for sponsors and vendors. Ensure compliance with ICH-GCP and regulatory standards. Mentor and support project team members. Qualifications: Bachelor’s degree in Life Sciences or related field. Minimum 5 years of clinical research experience, including 1+ year in project management. Strong therapeutic expertise in Cardiovascular and Cell and Gene Therapy. Proven leadership, communication, and problem-solving skills. Solid understanding of project financials and contract management. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen. Werden Sie Teil unserer Community von rund 86.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welche Rolle Sie bei IQVIA einsteigen, es erwartet Sie ein offenes, innovationsfreudiges Umfeld, in dem Sie sich viel bewegen können. Finden Sie heraus, wie Sie Ihre Talente und Ihre Leidenschaften bei IQVIA einbringen können. Im Bereich Commercial Engagement Services (CES) arbeiten wir eng mit unseren Life Sciences-Kunden zusammen und unterstützen sie mit flexiblen Vertriebs- und Personallösungen für nachhaltigen Erfolg am Markt. Dies umfasst insbesondere die Rekrutierung, das Training und die Steuerung des Vertriebsteams in Dienstleistungsprojekten bzw. in Arbeitnehmerüberlassung. Dabei differenzieren wir uns über integrierte Projektansätze entlang des IQVIA Lösungsportfolios, die wir individuell an die Kundenbedürfnisse anpassen und aus einer Hand anbieten. Komm in unser IQVIA-Team!Für ein spannendes Projekt im Bereich Hämatologie suchen wir Pharmaberater (m/w/d) zum nächstmöglichen Zeitpunkt Im Gebiet: Ingolstadt, Augsburg, München Das sind Deine Aufgaben: Identifizierung und Zuordnung der wichtigsten Accounts, Kunden und Entscheidungsträger in diesen Accounts aus dem Bereich der Hämatologie und Erstellung eines maßgeschneiderten Plans für jeden Account. Empfehlen und Entwickeln von maßgeschneiderten Lösungen für seinen Kunden und die Account-Netzwerke, denen der Kunde angehört. Durchführung von kompetenten Fachgesprächen nach VBS (Wertorientiertes Verkaufen) in den Fachgruppen der Hämato-Onkologen sowie Betreuung von ausgewählten onkologischen Pflegekräften. Umsetzung der Vertriebs- und Marketingstrategien der Geschäftseinheit. Dazu gehören der Außendienst und die Durchführung von Veranstaltungen, wie z.B. das Sponsoring der wichtigsten lokalen Veranstaltungen und Peer-to-Peer-Meetings. Erstellung und kontinuierliche Weiterentwicklung strategischer Analysen der betreuten Kunden (inkl. SWOT-Analyse, Patientenströme, Volumen dieser potenziellen Kunden) und Umsetzung der auf diesen Analysen basierenden Empfehlungen.  Aufbauend auf den bestehenden und Entwicklung neuer Zugangswege zu wichtigen Entscheidungsträgern, einschließlich persönlicher und virtueller Besuche für alle Kunden, unter Anwendung eines kundenspezifischen Multi-Channel-Ansatzes. Förderung und Umsetzung von Kontaktwegen für jeden Kunden, um eine optimale Frequenz über die vom Kunden bevorzugten Kanäle zu erreichen. Das bringst Du mit: Ausbildung zum geprüften Pharmareferenten oder wissenschaftliche Ausbildung (idealerweise Hochschulabschluss). 3-5 Jahre Berufserfahrung als erfolgreicher Pharmareferent/in in der Hämato-Onkologie. Die Fähigkeit und das Wissen, onkologische Kunden in gesundheitspolitischen Fragen zu beraten. Erfahrungen und Erfolge mit "Value Based Selling". Ein klares Verständnis von wertorientiertem Verkaufen und ausgezeichnete Verkaufsfähigkeiten in diesem Bereich. Bereitschaft, neue Zugangsmöglichkeiten über mehrere Kanäle zu entwickeln und umzusetzen. Hervorragende Zusammenarbeit und nachgewiesene Fähigkeit, mit unterschiedlichen Teams Ergebnisse zu erzielen. Hohe Lernflexibilität und Lösungsorientierung. Teamfähigkeit (Wir > ich). Ausgeprägtes strategisches, analytisches und kreatives Denken. Nachgewiesene Fähigkeiten zur Eigenverantwortung. Technische Affinität Das erwartet Dich bei uns: Ein attraktives Gehaltspaket plus Kundenprämien, vielfältige Corporate Benefits, betriebliche Altersvorsorge sowie 24/7 Unfallversicherung (auch für den privaten Bereich) und exklusive private Krankenzusatzversicherungen Ein top ausgestatteter Firmenwagen verschiedener Premiumanbieter mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des Modells  Eine moderne IT-Ausstattung für Deinen modernen digitalen Arbeitsplatz Unser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige Perspektive Wir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines Wohnorts  Eine hohe Übernahmequote durch unsere Kunden ermöglicht Dir den Karrierestart bei zukunftsweisenden und führenden Unternehmen der Pharmabranche und Medizintechnik-Branche Vielfältige und individuelle Weiterentwicklungsmöglichkeiten auch innerhalb von IQVIA (z.B. Führung, Key Account Management, Projektmanagement und vieles mehr) Wir begleiten Dich während Deiner Bewerbungsphase durch individuelle Betreuung/Vorbereitung bis zur Einstellung und auch darüber hinaus während des Beschäftigungsverhältnisses Unser Kunden-Netzwerk reicht vom Start-up Unternehmen bis zum Global Player. Gemeinsam mit Dir finden wir den richtigen Job für Dich! Starte Deine Karriere mit IQVIA! Dein besonders schneller Draht zu uns: Kandidaten-Hotline: 0621-84508113 oder sende uns gerne direkt Deine Bewerbung per Mail an: [email protected]  #LI-CES #LI-DNP #LI-SS2 #Pharmaberater #Biologie #Chemie #Pharmareferent #BTA #CTA #PTA #Onkologie #Hämatologie #Facharzt #Pharmazie #Pharma-Außendienst IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Research Nurse Location: York24 hours per week | 6 months contract (potential to be extended) | Start: July 2026 IQVIA is hiring an experienced Clinical Research Nurse to support a hypertension and cardiovascular clinical trial in York. What you’ll be doing:Perform a variety of complex clinical procedures on subjects including but not limited to vital signs, phlebotomy, administration of IP, ECG etcCollect, record, and report clinical data Assist in study enrollment by recruiting, screeningPerform clinical set-up and preparation for the study Perform data entry, data quality checking, and query resolutionWhat we’re looking for:Registered Nurse (active registration with NMC)Proven experience with phlebotomyMinimum 3 years’ Clinical Research Nurse experienceStrong clinical trial knowledge and hands-on skills (IP, ECGs, labs)Excellent organisation, communication, and attention to detailWhy IQVIA?Work with a global leader in clinical research on impactful studies in a supportive, professional environment. Apply now if you meet the essential experience criteria and are ready to make a difference in this space. #LI-HCPN #LI-CES #LI-DNP #LI-NS1 #LI-Onsite IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

OverviewIQVIA is seeking a highly skilled Senior Software Engineer specializing in React and Node.js to join our growing technology team. This role will contribute to building and enhancing scalable, high-performance web applications and data platforms that support IQVIA’s global business objectives and operational excellence. Key ResponsibilitiesDesign, develop, and maintain scalable web applications and data platforms in cloud environments (Azure/AWS).Contribute to application architecture decisions, ensuring alignment with business requirements and system scalability.Develop and implement microservices-based solutions with a focus on performance, modularity, and maintainability.Build secure, efficient, and well-documented APIs to support web applications and integrations.Collaborate with cross-functional teams, including product managers, architects, and stakeholders, to deliver technical solutions.Translate technical requirements into clean, maintainable, and efficient code.Participate in the full software development lifecycle—from requirements analysis to deployment and support.Conduct code reviews and follow best practices to ensure high-quality software delivery.Troubleshoot and resolve application issues, ensuring optimal performance and reliability.Stay current with emerging technologies and contribute to continuous improvement of development processes and tools.Required QualificationsBachelor’s degree in Computer Science or related field, or equivalent experience.5–8+ years of experience in software development, with a focus on web application development.Strong hands-on experience with React, Node.js, and modern JavaScript frameworks.Experience working with MongoDB, Snowflake, Databricks, or similar data platforms.Familiarity with Docker and Kubernetes for containerization and deployment.Experience with cloud platforms such as Azure and/or AWS.Understanding of API design, RESTful services, and secure coding practices.Experience implementing authentication mechanisms such as SSO.Strong problem-solving skills and ability to work in an agile, collaborative environment.Knowledge of modern software development tools, practices, and exposure to AI-driven technologies 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 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 $91,300.00 - $228,200.00. 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.

Senior Big Data Engineer The Role    We are looking for an experienced, innovative and highly motivated engineer who is capable of working independently to design, develop, and support data engineering solutions. This role requires a considerable focus on understanding our data we deal with as an organization, develop a better understanding of our data through profiling, take ownership of the solution design, work collaboratively with the wider engineering team to implement optimal solutions in a timely manner and ensure successful deployment and operation of the platform in production. Our platform helps solve complex business challenges pertaining to healthcare data such as mapping wide variety of healthcare drug and diagnosis data to standard coding frames. You will have the opportunity to solve complex engineering challenges and develop innovative solutions.  In your daily work you will be responsible for creation and delivery of a platform loading and processing millions of electronic medical records. The Team The Systems Engineering team is part of the Global Infrastructure & Operations (GIO) organisation and remains one of the most dynamic and fast-growing groups in the organisation. We are passionate about Agile software development and are among the strongest advocates for DevOps and Test-Driven Development (TDD). Our culture promotes autonomy and collaboration, empowering individuals to thrive within self-organising teams. Our work involves processing and analysing a wide range of patient-level healthcare data, which supports solving complex healthcare challenges — from retrospective clinical studies to disease progression modelling. In your daily activities, you will collaborate with a team of Architects who design effective solutions, and with the Quality Assurance team, which ensures the highest standards of software quality. The DataWe process over a billion records at a time; our engineers are responsible for the data analysis and construction and optimization of data flow processes. You will build data pipeline using ETL solutions for acquiring, processing and loading medical data into the Databricks. Core Responsibilities  Ability to oversee and guide junior and mid-level engineers, providing technical direction and mentoring to support their growth.Delegating tasks effectively, ensuring clarity of expectations and alignment with delivery goals.Ownership for the delivery of assigned workstreams, ensuring quality, timeliness, and accountability across the team.Build pipelines for processing big amount of medical dataParticipate in analysis, system design, development, deployment and maintenance Conduct peer code reviewsContribute to the definition and adoption of technical standardsCreate comprehensive automated unit and integration tests QUALIFICATIONS & SKILLS Qualifications Bachelor’s Degree in Information Technology, Software Engineering, Computer Science, Mathematics, or another related field  Technical skills and knowledge  6+ years of the following language: SQL, Python, Scala6+ years of experience in data engineeringStrong understanding of Databricks platformExperience with Big Data Batch processing and Azure Cloud ServicesPractical knowledge of Apache Spark ecosystem, including Delta and Parquet data formatsExperience with complex ETL design and implementationExperience with data analysis, data profiling, data integration, data quality, data warehousing, data reportingExperience with CI/CD automation processes and tools such as Jenkins/GitLabAdditional/nice to haveFamiliarity with AI-powered productivity tools such as Copilot or Cursor, and their practical use in day-to-day software development workflows (e.g. code generation, documentation, task automation, or debugging support).Experience working in an Agile environmentExperience with database design and modellingPrevious experience with healthcare or pharmaceutical data would be an advantageKnowledge of algorithms & design patterns and how to apply them effectively  Experience with large data volume (TBs’) processing   Personal skills and behaviours  Excellent analytical & troubleshooting skills Strong collaboration, written, and verbal skills Familiarity with project management concepts, specifically Agile/Scrum  Ability to present complex results in a clear language for both technical and non-technical audienceExperience collaborating with teams from Europe, with an understanding of cross-cultural communication and remote delivery dynamicsA great team player mindsetWhat we offer Work in a company with offices in over 100 countries around the world, listed on the American stock exchange (NYSE)Multi-terabyte databasesQuarterly work planning - goals and progress review every 90 daysTechnical trainingPossibility to participate in technical conferences within the countryFavourable employment conditions and benefitsIQVIA 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 188 700,00 zł - 350 200,00 zł. 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.

What will you be doing?Designing and developing ETL solutions to process big amount of medical dataActively collaborating with Architect Ensuring high quality supporting the design/redesign of solutions for big data & data warehouses projectsDelivering project estimationsParticipates in solution architecture research, PoCs, feasibility assessmentsClosely cooperates with teams and supports them in areas of collecting requirements, meeting with business stakeholders, providing consultation in defining/designing data flowsContinuously improving our data platform and reducing technical debtAdjusts/Extends the design of conceptual, logical data model, leveraging best practicesSupporting introduction of new tools and migration to Azure cloudDelivers the design of physical data modelsProvide mentorship to team members on data engineeringExecutes/Participates in development procesDefine development standards and promoting best practices What is required to get the job done?Experience:8+ years of experience in data engineering, ETL design, and implementation.5+ years of experience with batch processing.5+ years of experience in data analysis, profiling, integration, and reporting.Excellent knowledge of SQL and either Scala or Python (6+ years).Big Data Platforms: Strong experience with Cloudera or Databricks.Distributed Systems: Expertise in Hadoop Hive, Spark.Data Pipelines: Experience in optimising big data pipelines and ETL solutions.Cloud Platforms: Experienced with Azure.Technologies: Experience with Apache Spark and Kafka.Team Collaboration: Proven ability to work effectively in a team environment and technical lead in your field 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 217 300,00 zł - 461 700,00 zł. 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 OverviewDesigns/develops software solutions and business process solutions based on business needs and requirements using specialized domain knowledge and developed business expertise.Focuses on software quality standards for all aspects of work; establishes advanced software test standards and methods and conducts complex software tests.  Essential Functions• Designs/develops software solutions and business process solutions based on business needs and requirements using specialized domain knowledge and developed business expertise.• Works at all layers of the application stack including front-end user interface and backend development.• Analyzes and evaluates code issues and makes decisions within general parameters under broad supervision.• Leads projects and programs within own organization with moderate complexity and scope.• Focuses on software quality standards for all aspects of work; establishes advanced software test standards and methods and conducts complex software tests.• Performs code reviews and optimization of existing queries.• May assist in on-boarding new Software Engineers to the team Qualifications• Bachelor's Degree Computer Science, a related field, or equivalent experience Req•• IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is 177 500,00 zł - 329 600,00 zł. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job Overview The Medical Director for the Hematology-Oncology Center of Excellence provides strategic medical and scientific subject matter input to IQVIA in this therapeutic area informed by their training, experience and expertise. The activity of the medical director includes but is not necessarily limited to early engagement with potential customers, proposal development in response to RFPs, participation in client proposal bid-defense meetings, support at scientific conferences, participation in thought leadership activities, contribution as needed to the formulation of clinical development plans, providing medical director and subject matter expertise as a consultant throughout the research and development lifecycle and the duration of clinical trials, and engagement with colleagues as an internal reference SME for hematology-oncology. Greater independence is expected to be demonstrated over time for medical director activities under the supervision of the therapeutic area head and leadership team. Essential Functions Work independently under the supervision (direct or indirect) of the Hematology-Oncology Center of Excellence Head and COE Leadership team. Provide scientific and clinical advice to internal stakeholders developing proposals, including but not limited to: protocol design/ clinical development plan, insights on mechanism of action of the investigational product, mining data to address important clinical questions relevant to the study, reviewing protocol for scientific/regulatory soundness and feasibility, identification of target site and principle investigator profiles, anticipated patient recruitment, standards of care and competitive landscape. Maintain awareness of latest literature to keep abreast of scientific progress in hematology and oncology. Participate as needed in the preparation for and conduct of client meetings, such as early engagement, proposal discussion and bid defense meetings, post-award transition and governance meetings, and any other engagements necessary to support the goals and objectives of IQVIA. Provide advice, coaching, and preparation of project teams to align executional strategy to medical understanding and considerations. Collaborate as appropriate with key stakeholders and leaders in the organization, e.g., Business Development, Operations, Commercial Consulting Services, Real World Services, and other medical strategy leads across the Centres of Excellence Act as an internal and external consultant throughout the research and development life cycle and the duration of the clinical trials to provide scientific knowledge and clinical expertise to guide project teams Providing scientific knowledge and clinical expertise to guide sponsors in clinical development. Qualifications Oncologist (MD) with training in the relevant therapeutic area . Hematology training or expertise in addition to solid tumor experience is considered a plus. Typically requires a minimum of five to seven years of prior relevant experience. Practical knowledge in leading and managing the execution of processes, projects and tactics within research and development. Will have had a minimum of 3 years of experience outside of the training period with the biopharmaceutical industry either directly or indirectly. Professional Skills Excellent communication, presentation and interpersonal skills, including good command of English language (both written and spoken). Innovative and strategic thinker. Strong business acumen including confidence with financial considerations, excellent negotiation and influencing skills, and comfort working in scientific, operational, and business development environments. Excellent customer relations skills . Flexible and able to work in situations where specifications may or may not be well defined and willing to support collaborative work in other therapeutic areas when required. Confident and capable in the use of technology, applications and other media, e.g., databases and internet to research assess new opportunities, maintain currency of therapeutic and operational knowledge and competitive landscape. Proven ability to make decisions or provide guidance despite limited information, bringing clarity to disparate information to inform actions and drive results. Interpersonal Skills Ability to establish and maintain effective working relationships with co-workers, managers and clients. Maintains a positive outlook at work. Ability to establish and maintain effective working relationships with a wide network of individuals e.g. co-workers, managers and customers. Effective mentoring and training skills, fostering learning and knowledge sharing with colleagues. 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 $0.00 - $0.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

We are seeking Manager - Hematology Department to join IQVIA Laboratories at Valencia, CA.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Job Summary:Lead and supervise a hematology laboratory team to deliver high-quality, compliant, and efficient testing operations. This role drives day-to-day execution, supports staff development, advances process improvement, and ensures adherence to safety, quality, and regulatory requirements. What You'll Be Doing:Supervise daily laboratory operations and guide the team to meet workload, quality, and turnaround expectationsSet priorities, assign work, and monitor operational delivery across assigned laboratory work groupsSupport hiring, training, coaching, and performance management under the mentorship of managementOversee inventory, resource planning, and budget-aligned use of reagents and laboratory suppliesDrive safety, quality, and compliance practices, including timely resolution of CAPA and quality incidentsPartner with stakeholders to lead process improvement initiatives, evaluate vendor platforms, and strengthen laboratory performance metrics What We Are Looking For:Bachelor's Degree or equivalent combination of education and experienceTypically requires >5 years in regulated environment; >4 years of experience in a relevant discipline laboratoryIn depth knowledge of clinical testing procedures and applicable laboratory testing regulationsWorking knowledge of quality assurance and quality control principles, root cause analysis, and company-specific program requirementsOther Equivalent combination of education, training, and experience may be accepted in lieu of degree The Knowledge, Skills and Abilities Needed for This Role:Demonstrated ability to train and mentor others while navigating operational and people-related challengesAbility to assess and prioritize multiple tasks, projects, and competing demandsStrong written and oral communication skills with the ability to build effective working relationships with coworkers, managers, clients, and stakeholdersStrong understanding of laboratory operations, study setup, cross-functional dependencies, and occupational safety requirementsApplicable certifications and licenses as required by local regulations; Clinical Lab Scientist license preferred What We Offer You:We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.To learn more about our benefits, visit https://jobs.iqvia.com/benefits.If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $58,800.00 - $122,500.00. 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.

We are seeking Medical Laboratory Technician to join IQVIA Laboratories at Valencia, CA.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 performing routine hematology analysis and laboratory testing procedures in a regulated environment. This role supports accurate documentation, data review, laboratory operations, and compliance with standard operating procedures and applicable regulatory requirements. What You'll Be Doing:Perform routine analytical procedures and document all testing activities in accordance with standard operating procedures and regulatory requirementsReview routine laboratory data to confirm procedures are progressing according to expectations and results are within acceptable tolerancesIdentify unusual results or potential performance errors, document findings, and escalate concerns to senior laboratory personnelPrepare buffers, solutions, and data analysis results for upload to the laboratory information management system under the guidance of senior staffAssist with quality investigations, deviations, and implementation of laboratory procedure updates and process improvementsPerform calibration and maintenance of laboratory equipment as assigned and ensure all activities are properly documentedSupport onboarding and hands-on training of new laboratory staff in areas of proven competencyCommunicate clearly, accurately, and promptly with cross-functional stakeholders while supporting safety, quality, and 6S initiatives What We Are Looking For:Bachelor's Degree or equivalent combination of education and experience. Some College of American Pathologists and Clinical Laboratory Improvement Amendments laboratory locations may require a Bachelor of Science in a chemical, physical, biological or clinical laboratory science, medical laboratory technology or cytotechnology6 months experience in a regulated laboratory environment preferredProficiency with relevant laboratory techniques and routine analytical proceduresExperience working with automation or specialized laboratory equipment and preparing data for the laboratory information management systemOther Equivalent combination of education, training, and experience may be accepted in lieu of degreeMedical Laboratory Technician license is required The Knowledge, Skills and Abilities Needed for This Role:Working knowledge of applicable regulatory standards such as Good Laboratory PracticesStrong attention to detail and accuracy in laboratory documentation, calculations, and data reviewAbility to manage multiple tasks simultaneously and collaborate effectively with internal stakeholdersGood computer skills using Microsoft Outlook, Word, and ExcelKnowledge of laboratory safety, infection control procedures, standard precautions, and hazardous chemical handlingAbility to lift up to 50 lbs, frequent standing and walking, occasional sitting, close eye work requirement (computer, typing, reading small prints). Physical demands vary depending on assigned work area and work tasks. Occasional exposure to cold temperatures. What We Offer You:We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.To learn more about our benefits, visit https://jobs.iqvia.com/benefits.If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $42,700.00 - $89,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

◆Hiring Managerからのメッセージ今回のポジションでは、クライアントの課題に深く向き合いながら、データとコミュニケーションを通じてIQVIAが提供する海外データサービスの価値を最大化し、お客様に届けていく役割を担っていただきます。私たちのチームは、単なる顧客対応にとどまらず、「どうすればお客様にとってより価値ある活用ができるか」を主体的に考え、提案していくパートナー型のクライアントサポートを大切にしています。お客様の意思決定に直接貢献できる点が、この仕事の大きなやりがいです。顧客志向のマインドとコミュニケーション力があれば、ヘルスケアやデータ領域の経験がなくても、入社後の体系的なサポートを通じて着実にキャッチアップできる環境があります。また、チームメンバーが常にサポートを行いますので、未経験領域にチャレンジしたい方にも安心してご活躍いただけます。さらに、本ポジションで扱うデータやサービスは、医療・製薬業界の重要な意思決定を支える基盤となるものです。その先には患者さんや社会全体への価値提供があり、「自分の仕事が社会に貢献している」という実感を持てる点も大きな魅力です。顧客に寄り添い、価値を共に創り上げていきたい方、英語やデータを活用しながらスキルの幅を広げたい方、そして社会にインパクトのある仕事に挑戦したい方と、ぜひ一緒に働けることを楽しみにしています。　 ◆こんな方におすすめ！・クライアント志向・提案力を活かしたい方・英語を使ってグローバルに働きたい方・データやテクノロジーに興味がある方（未経験歓迎）・チームで協力しながら成果を出したい方・営業・カスタマーサクセス・サポート経験を活かしたい方・ヘルスケア分野での社会貢献に興味がある方 ーーーーーーーーーーーーーーーーーーーーーーーーーーーーーーーーーーー【ポジション名】Client Service representative 【会社紹介・ビジョン】私たちIQVIAは、ヒューマンデータサイエンスの先駆的な企業として、医療・ヘルスケアの前進に取り組む皆様をIQVIAならではの革新的なソリューションによってご支援することで、「誰もが、より健康に自分らしく生きられる社会」の実現を目指しています。世界最大規模を誇る医療・ヘルスケア関連データを基盤に、人・データ・サイエンスを融合させた見地から、未だ満たされない治療ニーズに応える、新たな医薬品や医療機器の開発と市販化、厳格化する規制やコンプライアンスへの対応、持続可能な医療システム推進の支援など、患者さんをはじめとするすべての人々のために、より良い未来へと医療・ヘルスケアを前進させていく力となることが、私たちの使命です。世界100以上の国と地域で約9万人が活動するIQVIAの日本法人として、IQVIAジャパンでは約6,000人が一丸となり、この使命に向かって日々、力を尽くしています。 【部門について】海外事業部Global Market Insights チームが開発する海外データサービスを、主なクライアントである日本の製薬企業に提案しています。 「営業」「マーケティング」「クライアントサービス」「契約業務」の4つのチームで構成されており、今回のポジションは、「クライアントサービス」の業務を担当頂きます。 業務内容 ■ クライアントマネジメント ・顧客との関係構築・定期コミュニケーション ・利用状況の分析と活用促進、改善提案 ・契約更新・アップセルの推進 ・新規施策の導入支援 ・グローバルチームとの連携・報告 ■ サポート・運用 ・海外データサービス製品に関するお問い合わせ対応 ・顧客向けトレーニングの企画・資料作成・実施 ・データ作成・品質チェック・納品 ・システム／アクセス関連の対応 ・システム／アクセス関連の対応 必須条件•    日本語ネイティブレベル、英語ビジネスレベル（文書作成・会議対応）•    クライアントファーストな思考 歓迎条件•    顧客対応経験（営業/顧客サポート等）•    ヘルスケア業界経験•    データやテクノロジーへの興味関心 勤務地•    東京 雇用形態・勤務時間・福利厚生・休日休暇•    雇用形態：正社員•    勤務時間：9:00-17:00•    フレックス勤務：あり•    在宅勤務制度：あり•    福利厚生：法定内（社会保険制度）・法定外（IQVIA独自制度）の両面から充実した福利厚生制度あり•    受動喫煙対策：あり•    休日休暇：年次有給休暇、夏季休暇、病気休暇、特別休暇、女性特別休暇、育児介護休暇、看護休暇·など•    試用期間：あり（通常６か月） 給与・待遇•    給与：当社規定により優遇します•    昇給：あり•    賞与：あり•    時間外手当：あり 選考プロセス•    書類選考～3次面接 応募方法•    Workdayより応募書類をご提出ください 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 Description SummaryJob OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential Functions• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.• Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.• Assist with periodic review of study files for completeness.• Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.• Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.• Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.• May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.Qualifications• High School Diploma or equivalent Req• 3 years administrative support experience.• r.• Equivalent combination of education, training and experience.• Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.• Written and verbal communication skills including good command of English language.• Effective time management and organizational skills.• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.• Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.• Knowledge of applicable protocol requirements as provided in company training.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.

Brief DescriptionUnder close guidance or supervision, responsible for performing existing operational processes and procedures on vaious platforms, including but not limited to hadoop and oracle. Obtain the necessary knowledge and experience related to patient level data assets such as oncoloty and ambulatory electronic medical records, lab data and health plan enrollment and claims data. Role and ResponsibilitiesExecute and perform scripts related to releases, projects, or fixes supporting new functionality, quality assurance and regression.Perform data trend checking, analyze data and investigate on data points that are out of threshold to find/present appropriate solutions/conclusions.Document, communicate and analyze data discrepancy.Identify test effort needed to appropriately validate data variance.Effectively articulate findings or results, data trends and able to come up conclusions.Query and analyze large amount of data based on the given task, business requirement and issue in question.Create SQL related queries to verify published data requests, retrieve specific data sets and results as needed for validation purposes.Job QualificationsBachelor’s Degree in Computer Science/Information Technology/Engineering or equivalent.At least a minimum of five (5) years of work experience in related field is required.    Demonstrates strong problem solving and business analytical skills.Demonstrates strong understanding of complex concepts and processes. Has initiative to learn and is self-motivated to attend to client needs and resolve concerns with minimal supervision.Ability to communicate effectively with various levels of the organization.Strong organizational and time management skills are required.Proficiency in MS Office applications especially in Excel (perform data quality analysis) is essential. Good team playerHealthcare knowledge would be a plusKnowledge in SQL programming (Basic to advanced) (T- SQL or PL/ SQL), Hadoop Technology Stack (Spark (Scala based), HIVE, Python, Pyspark, Hue-Impala, SQuirreL is preferred but not requiredAmenable to work on Hybrid Set up in Mckinley, TaguigAmenable to work on Night shiftIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Role Purpose: Under close guidance or supervision, responsible for creating and maintaining the IQVIA outlet database. Job Description: Perform daily maintenance of outlet master file for US production. Solicits, gathers, and validates information from different sources to identify accuracy of outlet reference record. Perform daily bridging of outlet sales recycles to IQVIA database. Response to outlet related queries. Work on client specific projects with varying nature and business rules. Responsible for maintaining work allocations sheets containing client-required details that varies from one project to another. Escalate issues to the project lead or team lead. Perform functions as directed by the project lead/supervisor/manager. Minimum Education, Experience, & Specialized Knowledge Required: Bachelor’s degree in any science and technology field Strong interpersonal, written, and communication skills. Strong customer focus, an attention to detail and excellent analytical and problem-solving skills. Proficient in the use of Microsoft office application. Ability to work under time constraints and under minimum supervision. Willing to work in the night shift. Job Requirements: Bachelor’s degree in any science and technology field Strong interpersonal, written, and communication skills. Strong customer focus, an attention to detail and excellent analytical and problem-solving skills. Proficient in the use of Microsoft office application. Ability to work under time constraints and under minimum supervision. Willing to work in the night shift. 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.

External Job DescriptionRoles and Responsibilities Ensures that the appropriate processes are adequately documented and followed across all systems. Converts data received from the data suppliers into IQVIA standard format as per instructions. Received sales, product, manufacturer, and customer files are processed using the relevant IQVIA applications and procedures to produce the relevant coding for the period. Oversees all quality assurance testing and ensures that all testing is carried out prior to deliverable dispatch. Responsible for timely completion of all QC-related production tasks including the off-cycle reports and other relevant tasks. Conducts various checks to capture any data anomaly prior to the release of client deliverables. Maintains the data quality by analyzing various reports that generate transactions which have potential issues. Performs data checks by analyzing results and trends. Provides impact analysis of identified data corrections. Understands and can effectively communicate routine database processes. Serves as subject resource on relevant production area, answering queries. Reviews problems arising during the process and ensures successful resolution. Communicates actively with other departments/ functions to inform of task status or to resolve problems. Escalates issues requiring second-level support to appropriate individuals using the established call escalation procedures. May provide input for new system development, including requirement gathering, UAT and implementation. Contributes on identifying process improvement opportunities. Perform functions as directed by the Manager. List of required skills for this role: Associate degree, diploma, or equivalent Proficiency in Windows application (Word and Access) Knowledge in Microsoft Excel.  Good interpersonal, written, and verbal communication skills Strong customer focus, attention to details, analytical and problem-solving skills Ability to carry out analysis and information gathering to resolve problems on routine matters. Ability to work under time constraints and changing work volumes. Willing work on flexible schedule and can render OT on the holiday. 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.