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SantenPosted 2 weeks ago

Global Medical Affairs Research Grant & Study Manager

$78,863–$108,436 year

HybridSt Albans, England, United Kingdom

Full TimeLargePHARMA

Job Summary

Lead global Investigator-Sponsored Studies (ISS/IST) and research grant programs from proposal intake through payment oversight, ensuring execution aligns with GCP, ICH guidelines, and company policies. Manage end-to-end lifecycle operations for Phase IV studies, registries, observational research, and real-world evidence initiatives while maintaining inspection-ready documentation. Coordinate scientific reviews, contracting, milestone tracking, and reporting for investigator-led programs across multiple regions. Partner with Clinical Development, Compliance, Legal, and external stakeholders including CROs, academic institutions, and key opinion leaders to drive evidence-generation strategy and facilitate seamless transitions from Phase III to post-approval research. Support study outcomes through publications and presentations to advance scientific knowledge and patient outcomes.

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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