Associate Director, Medical Advisor, EU West
New
B
BridgeBioBiopharma, rare disease
Remote - FranceFull-TimeDirector
Salary not disclosed
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Job Details
- Languages
- Fluent French and professional English, both written and spoken
- Experience
- At least 3-5 years of Medical Affairs experience in the pharmaceutical or biotechnology industry, including meaningful experience in France
- Required Skills
- Project Management
Requirements
- Hold an MD, PharmD, PhD, or another advanced scientific or healthcare degree.
- Have at least 3-5 years of Medical Affairs experience in the pharmaceutical or biotechnology industry, including meaningful experience in France.
- Demonstrate ability to engage healthcare professionals in high-quality scientific exchange and convert field insights into medical actions.
- Have experience developing and executing country medical plans, preferably in a launch or pre-launch setting.
- Understand the French healthcare system, hospital and expert-center environment, and compliance framework for healthcare stakeholder interactions.
- Have strong scientific writing, presentation, and data interpretation skills.
- Have project management skills and the ability to manage several priorities in a small, fast-moving organization.
- Be fluent in French and professionally proficient in written and spoken English.
- Preferred: experience in rare diseases and in skeletal dysplasia or pediatrics, neuromuscular disease, endocrinology, or mineral metabolism.
- Preferred: experience with real-world evidence, investigator-sponsored research, publications, or early access programs.
Responsibilities
- Co-develop and execute the France Medical Affairs plan for the three portfolio programs, including priorities, milestones, KPIs, resource needs, and budget assumptions.
- Maintain expertise in the diseases, patient journeys, standards of care, competitive environment, and emerging evidence, and translate data into relevant scientific narratives for French stakeholders.
- Build peer-to-peer relationships with experts, multidisciplinary care teams, scientific societies, rare-disease networks, and patient organizations.
- Map and segment relevant centers and stakeholders, characterize referral and treatment pathways, and help quantify patient populations and unmet medical needs across France.
- Capture, analyze, and communicate actionable field insights, and show how validated insights inform strategy and execution.
- Deliver scientific exchange and education, including advisory boards, expert meetings, congress activities, and internal training.
- Contribute to evidence generation, including real-world evidence, registries, epidemiology, outcomes research, collaborative studies, and investigator-sponsored research.
- Support launch readiness by clarifying unmet need, patient identification and referral pathways, multidisciplinary care requirements, and evidence gaps.
- Review scientific, educational, market access, and promotional materials for accuracy, fair balance, and consistency with approved information and company standards.
- Partner with cross-functional teams and report adverse events, product complaints, and other safety information within required timelines.
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