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The Associate Director Medical Affairs will play a strategic role in supporting scientific and medical initiatives across marketed products and pipeline programs. This position partners with cross functional teams to ensure alignment between clinical data, therapeutic strategy, and business objectives. The role focuses on developing high quality scientific communications and driving medical education initiatives. The ideal candidate will bring strong expertise in clinical data interpretation and stakeholder engagement. This is a highly visible role contributing to improved patient outcomes and product value.
Job Responsibility:
Support and execute medical affairs strategies for assigned products and ongoing projects
Act as a subject matter expert for internal teams including medical and commercial stakeholders
Develop and deliver scientific training on disease state, mechanism of action, and clinical data
Create and contribute to scientific materials including publications, presentations, and healthcare professional content
Collaborate with cross functional teams including research and development, regulatory, and commercial teams
Support planning and execution of medical education initiatives such as symposiums and training programs
Maintain up to date knowledge of clinical data, treatment guidelines, and therapeutic area advancements
Assist in managing project timelines, deliverables, and budget considerations
Engage with external experts and support scientific exchange and relationship development
Requirements:
Advanced degree such as PhD PharmD or MD in a scientific discipline
Minimum five years of experience in pharmaceutical or biotechnology industry
Strong understanding of medical affairs functions and processes
Knowledge of clinical trial methodology and regulatory requirements
Experience developing scientific communications and medical education materials
Ability to work effectively in a cross functional matrix environment
Strong communication, analytical, and organizational skills
Experience interacting with healthcare professionals and internal stakeholders
Nice to have:
Experience in medical aesthetics
Experience designing clinical trial protocols
Prior involvement in congress presentations or scientific symposia
Experience with external expert engagement strategies