Clinical FSP Go-to-Market

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human...

Clinical Research Associate 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. Clinical Research Associate 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,...

IQVIA Belgium seeks a Director, Clinical FSP Go to Market/TSL to lead the go-to-market strategy for FSP solutions across regions and translate capabilities into compelling client narratives.This role partners with Sales, BD and Operations to design differentiated, feasible delivery models, drive early engagement, support RFIs and RFPs, and grow FSP-based...

As a Principal Biostatistician, you will provide strategic statistical leadership for Oncology clinical trials, with a particular focus on hematological malignancies including multiple myeloma, leukemia, and lymphoma. You will work closely with cross-functional teams to deliver high-quality statistical support across the clinical development lifecycle,...

Job Overview Acts as Lead Medical Writer on most types of writing projects. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Performs Senior Review of straightforward medical writing deliverables. Negotiates timelines and discusses/resolves customer...

Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions.Influence and contribute to clinical development plans, collaborate with cross-functional team for...

The FTE Medical Writer will serve as an integrated member of the team, delivering medical writing services for the development of clinical documents, including Clinical Trial Reports (CTRs), Trial Design Outlines/Clinical Trial Protocols (TDOs/CTPs) and CTP amendments, Briefing Books, Investigator’s Brochures (IBs) and IB updates, Biomarker Reports, and...

Clinical Research Associate 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 join our Sponsor dedicated team CRA (Junior -...

About the role Are you an experienced Clinical Project Manager who enjoys developing others, building strong teams, and helping colleagues succeed? We are looking for a CPM Line Manager to join our cFSP team and provide leadership, coaching, and functional oversight to an assigned group of Clinical Project Managers. This opportunity could suit an established...