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** Pour être éligible à ce poste, vous devez résider dans le même pays/la même région commerciale où se trouve l'emploi ** Sous supervision modérée, exécute les activités liées à la faisabilité, à l’identification des sites, aux affaires réglementaires, au démarrage (mise en rou
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 Gesundhei
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 Gesundhei
Join IQVIA and help drive healthcare forward. We are seeking a Global Key Account Director to lead strategic relationships with designated global pharmaceutical clients. In this highly visible commercial leadership role, you will develop trusted executive partnerships, shape acc
IQVIA is seeking a Clinical Research Associate II with independent on-site monitoring experience to join our team. We are looking for professionals with experience in one or more of the following therapeutic areas: - Central Nervous System (CNS) - Cardiovascular - Obesity - MASH
Location: Remote/Virtual Hours: Estimated 10–16 hours per month Role: Clinical Independent Rater for Clinical Trials The CIR plays a key role in ensuring the integrity and reliability of clinical trial data. This position involves reviewing scales administered by raters to confi
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP-1), diabetes, GI, MASH/NASH, dermatology, or respiratory: Job Overview: Perform monitoring and site management work to ensure that sites
With approximately 70,000 employees in more than 100 countries, IQVIA is in a truly unique position to be able to support companies seeking to improve real-world patient outcomes and enhanced clinical trial outsourcing through treatment innovations, care provision and access. Wit
IQVIA is seeking a CRA 2 with a minimum of 1.5 years of on-site oncology monitoring experience: Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Pr
The IQVIA Global Health Economics and HTA team includes highly qualified multi-disciplinary professionals in a variety of health economics, statistics, life sciences and epidemiology-related disciplines based across multiple geographies worldwide. We help our customers design and
Position Title: Mobile Nurse (LPN/LVN) – Per Diem, In-Home Services Location: Various U.S. locations (local travel within designated geographic area) About the Role: IQVIA’s In-Home Clinical Solutions team seeks a qualified and dedicated Mobile Licensed Practical Nurse (LPN) or
Are you looking to develop your career in laboratory automation and drug discovery? IQVIA Discovery Sciences in Cambridge is seeking an Associate Technical Specialist to support our Sample Management team, helping to deliver critical laboratory operations that accelerate researc
For candidates able to start before December 2026, a discretionary sign‑on bonus of up to 4,300 EUR may be offered, with the final amount confirmed at offer stage, subject to role level and relevant experience. IQVIA Belgium is looking for talented and motivated team member to j
IQVIA is seeking a Clinical Research Associate II with independent on-site monitoring experience to join our team. We are looking for professionals with experience in one or more of the following therapeutic areas: - Immunology/Gastroenterology (IM/GI) - Dermatology - Women's He
Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions • Perform site monitoring
Job Overview: Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions: • Perform site monitorin
Regulatory & Start Up Specialist 1, cFSP - Global Support Essential Functions • Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necess
Are you interested in joining a team trying to build intelligent connections across the healthcare ecosystem to enable smarter decisions that reduce costs and drive better patient outcomes? We leverage our unparalleled expertise to provide comprehensive data solutions, actionable
Job Overview IQVIA MedTech is seeking an experienced Clin Ops leader to manage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and meeting project objectives. Support senior leadership on re
Shape the future of drug discovery through automation, innovation and technical expertise. Are you passionate about laboratory automation, sample management and solving complex technical challenges? Do you thrive in an environment where you can influence how work is done, mento
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