This strategic role connects science to business by translating safety evidence into actionable plans that inform decision-making
Job Summary
This strategic role connects science to business by translating safety evidence into actionable plans that inform decision-making.
The incumbent will lead the strategy and execution of Integrated Evidence Generation Plans with a focus on real-world safety studies.
Candidates must possess a strong medical background and 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.
Skills & Requirements
Must-have
Medical degree or PhD/PharmD preferred
10+ years leading clinical projects
Experience in patient safety and drug development
Knowledge of GCP and GVP regulations
Ability to analyze complex safety data
Nice-to-have
Strong cross-functional collaboration skills
Proactive hands-on attitude
Excellent communication with KOLs
Ability to work with minimal supervision
Innovative problem-solving mindset
Key Requirements
Medical Degree (MD) preferred
Minimum 10 years pharmaceutical experience
Working knowledge of GCP and GVP
Clinical development or medical affairs background