Lead and execute the regional Medical Affairs strategy across the Americas, aligned with global medical strategy and regional business priorities
Provide scientific and clinical leadership for marketed and pipeline orthopedic products, ensuring accuracy, integrity, and compliance of all medical communications
Oversee evidence generation activities, including clinical studies, registries, post-market surveillance, and real-world evidence initiatives
Establish and maintain strong relationships with key opinion leaders, investigators, and professional societies across the Americas
Partner cross-functionally with R&D, Regulatory, Quality, Marketing, and Commercial teams to support product lifecycle decisions and regional strategies
Ensure regional Medical Affairs activities comply with all applicable laws, regulations, internal policies, and ethical standards
Lead, develop, and inspire a high-performing regional Medical Affairs team, fostering a culture of scientific excellence and collaboration
Provide medical input into risk management, safety surveillance, and issue management activities

Advanced degree in Medicine (MD), Pharmacy (PharmD), PhD, or equivalent life sciences discipline
Typically requires 10-12 years of experience in Medical Affairs within the pharmaceutical or medical device industry, including regional or multi-country leadership
Demonstrated people leadership experience, including managing managers and senior professionals
Strong knowledge of regulatory, compliance, and ethical requirements governing Medical Affairs activities
Excellent strategic thinking, communication, and stakeholder-management skills
Fluency in English required; Portuguese and/or Spanish strongly preferred.
Travel: Up to approximately 30 –40% regional and international travel.

Director, Medical Affairs, Can & LATAM

Key skills