This strategic role connects science to business by translating safety evidence into actionable plans that inform decision-making across the product lifecycle
Job Summary
This strategic role connects science to business by translating safety evidence into actionable plans that inform decision-making across the product lifecycle.
The incumbent will lead the strategy and execution of Integrated Evidence Generation Plans, including planning and prioritizing real-world studies focused on safety aspects.
Candidates must possess a strong medical background with at least 10 years of experience leading scientific projects within the pharmaceutical or biotech environment.
Matching Summary
This strategic role connects science to business by translating safety evidence into actionable plans that inform decision-making across the product lifecycle.
Skills & Requirements
Must-have
Medical degree or PhD/PharmD
10+ years pharmaceutical experience
Clinical development and patient safety expertise
Real-world evidence study design
Safety signal management and benefit-risk assessment
GCP and GVP knowledge
Nice-to-have
Strong cross-functional collaboration skills
Experience with Key Opinion Leaders (KOLs)
Ability to travel 10-20% of time
Proactive hands-on attitude
Excellent analytical and communication skills
Key Requirements
Medical Degree preferred; PhD or PharmD accepted
Minimum 10 years leading clinical/scientific projects
Working knowledge of GCP and GVP regulations
Experience in clinical development or medical affairs