Associate Director, Medical Affairs & Regulatory/Pharmacovigilance

About the role

Join Novo Nordisk Philippines as the Associate Director leading Medical Affairs and Regulatory/Pharmacovigilance. You will sit on the affiliate Leadership Team, shaping scientific communication and regulatory strategy to support sustainable growth and patient impact in the Philippines.

Key responsibilities

• Provide medical and regulatory insights for short‑ and long‑term strategic planning.
• Lead accurate, credible scientific communication across all channels and audiences.
• Establish strong KOL governance and engage with local health authorities.
• Build and share scientific and medical knowledge internally and externally.
• Drive education initiatives, coordinate publication and congress strategies, and represent the company at scientific meetings.
• Align local implementation of global and regional medical strategies with national product plans.
• Oversee regulatory submissions, pharmacovigilance operations, and compliance, maintaining relationships with health authorities.
• Lead patient‑safety functions, ensuring pharmacovigilance and medical‑device vigilance systems meet all regulatory requirements.

Required profile

• Licensed physician or a degree in biomedical sciences.
• Post‑graduate qualification is desirable.
• Minimum 10 years of relevant experience in medical affairs, regulatory affairs, or pharmacovigilance.

Required skills