This role provides strategic medical leadership to translate safety evidence into actionable plans that inform decision-making and enable differentiated strategies for autoimmune therapies
Job Summary
This role provides strategic medical leadership to translate safety evidence into actionable plans that inform decision-making and enable differentiated strategies for autoimmune therapies.
The incumbent will collaborate with internal stakeholders and external partners to lead the strategy and execution of Integrated Evidence Generation Plans focusing on safety aspects and outcomes.
Candidates must possess a strong medical/scientific background with at least 10 years of experience leading scientific projects within the pharmaceutical or biotech environment.
Matching Summary
This role provides strategic medical leadership to translate safety evidence into actionable plans that inform decision-making and enable differentiated strategies for autoimmune therapies.
Skills & Requirements
Must-have
Pharmaceutical drug development experience
Patient safety expertise
Real-world evidence study design
Safety signal management
Cross-functional collaboration
Nice-to-have
Strong communication skills
Proactive problem solving
Ability to work with minimal supervision
Experience with KOL engagement
Continuous learning mindset
Key Requirements
Medical Degree preferred (MD, PhD, PharmD)
Minimum 10 years in pharma/biotech
Knowledge of GCP and GVP regulations
Experience in clinical development or medical affairs