Global Medical Affairs Research Grant & Study Manager
$90,794–$124,842 year
HybridParis, Île-de-France, France
Job Summary
Lead global Investigator-Sponsored Studies (ISS/IST) and research grant programs by owning the end-to-end lifecycle, coordinating proposal intake, scientific review, governance, contracting, and milestone tracking. Ensure studies execute in compliance with policies and regulations while maintaining inspection-ready documentation. Drive Medical Affairs evidence generation by managing Phase IV studies, registries, and real-world evidence initiatives across multiple regions. Monitor timelines, budgets, and deliverables to support seamless transitions from Phase III programs to post-approval research. Partner with Clinical Development, Compliance, Legal, and external stakeholders including investigators, KOLs, and CROs to advance scientific knowledge.
Required Qualifications
- 5+ years of experience in Medical Affairs, Clinical Research, Clinical Operations, Evidence Generation, or a related field
- Strong experience managing Investigator-Sponsored Studies (ISS/IST) and research grant programs
- Proven expertise in research grant governance, including review processes, contracting, milestone management, reporting, and payment oversight
- Demonstrated experience in Medical Affairs evidence generation, including Phase IV studies, registries, observational research, and real-world evidence programs
- Experience collaborating with Clinical Development teams and supporting the transition from Phase III clinical programs to post-approval research
- Experience working with investigators, academic institutions, KOLs, CROs, and external research partners
- Bachelor's degree in Life Sciences, Pharmacy, Nursing, Public Health, or another relevant scientific discipline
- Strong working knowledge of GCP, ICH guidelines, and clinical research regulations
- Fluent English communication skills
Desired Qualifications
- Advanced scientific degree (PhD, PharmD, MPH, MSc) preferred
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