IQVIA
Open positions
Regulatory Affairs Officer
Job Overview Supports peer Publishers/Publishing Leads and eCTD Lead in the preparation of study reports, submissions, or other documents for either internal IQVIA customers or external clients by providing quality…
Site Contract Manager
Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company sponsored and/or investigator-initiated studies through direct negotiation with clinical trial sites or via oversite of a…
Regulatory Affairs Manager, Europe Biologic SME
At IQVIA, our Global Regulatory Affairs team partners with pharmaceutical and biotechnology companies worldwide to navigate complex regulatory environments and accelerate access to innovative therapies. We are seeking…
Regulatory Affairs Manager – Ad/Promo SME & Product Specialist
At IQVIA, our Global Regulatory Affairs team partners with pharmaceutical and biotechnology companies worldwide to navigate complex regulatory environments and support the successful development, approval and lifecycle…
Site Contract Manager - cFSP, Hungary
Why Join Clinical Functional Service Partnerships (CFSP)? At IQVIA, our Clinical Functional Service Partnership (CFSP) models offer the best of both worlds: the opportunity to work as an integrated member of a leading…
Assistant General Counsel, Healthcare Compliance and Investigations
IQVIA seeks an experienced attorney to serve as Assistant General Counsel, Healthcare Compliance and Investigations. Reporting to the SVP, Deputy General Counsel and Chief Compliance Officer, this attorney will provide…
Associate Program Director, Regulatory Affairs
At IQVIA, we help life sciences organizations accelerate the development and commercialization of innovative therapies that improve patient outcomes worldwide. We are seeking an experienced Associate Program Director,…
Associate Program Director, Regulatory Affairs
At IQVIA, we help life sciences organizations accelerate the development and commercialization of innovative therapies that improve patient outcomes worldwide. We are seeking an experienced Associate Program Director,…
Legal Specialist/Attorney 1
Professional Profile Highly experienced legal professional with extensive background supporting corporate legal departments, in-house counsel, and senior legal leadership across complex legal, compliance, governance,…
VP/Senior Director, Neurology Regulatory Affairs
Internal Job Description MCRA is part of IQVIA MedTech. As a trusted CRO and advisory partner, IQVIA MedTech and MCRA deliver integrated lifecycle solutions for the medical device and diagnostics industry. Together, we…
Senior Regulatory Affairs Specialist
Shape the future of regulatory excellence at IQVIA At IQVIA, we work to advance healthcare by helping our clients bring safe, effective medicines to patients. As a Senior Regulatory Affairs Specialist, you will play a…
Legal Counsel EMEA M&A
Meet the Team You’ll be joining a diverse, passionate, and high-performing international legal team that thrives on solving complex challenges through working on cutting-edge projects that shape the future of…
Site Contract Manager
Job Overview: Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor’s…
Vice President, MedTech Cardiovascular Regulatory Affairs
MCRA is part of IQVIA MedTech. As a trusted CRO and advisory partner, IQVIA MedTech and MCRA deliver integrated lifecycle solutions for the medical device and diagnostics industry. Together, we support innovation from…
Director, Regulatory Affairs – Regenerative Medicine & Biologics Quality
MCRA is part of IQVIA MedTech. As a trusted CRO and advisory partner, IQVIA MedTech and MCRA deliver integrated lifecycle solutions for the medical device and diagnostics industry. Together, we support innovation from…
Global Regulatory Affairs Manager (homebased)
No visa or accommodation sponsorship You will be responsible for regulatory activities required at a country level for pharmaceutical products, including maintenance and approvals, marketing authorization transfers,…