The role involves advising and managing medical activities to ensure scientific validity and ethics while enhancing local data generation for product life-cycle management
Job Summary
The role involves advising and managing medical activities to ensure scientific validity and ethics while enhancing local data generation for product life-cycle management.
Key responsibilities include designing and managing Non-interventional Studies, developing publication plans, and providing medical input on business decisions and marketing strategies.
The position requires acting as a key partner in crisis management, reviewing safety events, and ensuring all external communications meet strict medical compliance standards.
Matching Summary
The role involves advising and managing medical activities to ensure scientific validity and ethics while enhancing local data generation for product life-cycle management.
Skills & Requirements
Must-have
Fluent English spoken and written
Clinical trial knowledge
Lung cancer therapeutic area expertise
Microsoft Office software proficiency
3 years clinical practice in Tier 3 hospitals
Nice-to-have
Strategic thinking and analytic skills
Strong business acumen
Proactive planning and result oriented
Excellent teamwork and collaboration
Customer focus
Key Requirements
Master degree in Clinical Medicine preferred
3 years clinical practice experience required
Experience in multinational pharmaceutical companies preferred