At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill®, Compeed®, Solpadeine®, NiQuitin®, ACO®, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.
Join us on our One Perrigo journey as we evolve to win in self-care.

DESCRIPTION OVERVIEW

The Global Medical Director for Women’s Health will provide strategic medical leadership to advance the company’s portfolio in the women’s health category. This role encompasses the development and execution of medical affairs activities, clinical strategies, healthcare professional (HCP) engagement, claims strategy and substantiation, as well as innovation and portfolio protection/maintenance. The incumbent will collaborate cross-functionally to ensure alignment with commercial objectives and regulatory requirements, driving the delivery of scientifically robust and commercially viable products.

EXPERIENCE REQUIRED

Qualifications:

• Preferred: Medical degree (MD) or relevant life science scientific degree – PharmD, Pharmacist, PhD, MSc etc.
• Extensive experience in medical affairs, preferably in women’s health.
• Proven track record in medical strategy, clinical development, and HCP engagement.
• Strong understanding of regulatory requirements and evidence generation.
• Excellent communication and interpersonal skills.
• Demonstrated leadership in matrix environments.

Preferred Qualifications:

• Global experience across multiple markets.
• Clinical or research background in women’s health.
• Familiarity with digital health technologies.

• Develop and implement a comprehensive global medical affairs strategy for the women’s health portfolio.
• Provide subject matter expertise on women’s health products, diseases, and public health implications.
• Support medical communications, publication planning, and congress strategy.
• Identify evidence gaps and oversee the design and execution of Phase IIIb/IV clinical trials, observational studies, and other evidence generation activities.
• Oversee the strategy and design of scientific/clinical studies for claim substantiation.
• Write and review clinical components of the core regulatory dossiers and support Health Authority interactions.
• Establish and maintain strong relationships with KOLs, professional societies, and other stakeholders.
• Develop and substantiate product claims based on robust scientific evidence.
• Collaborate with cross-functional teams to identify opportunities for innovation and lifecycle management.
• Provide input and due diligence for business development and acquisition projects.
• Monitor the competitive landscape and emerging scientific trends.
• Ensure all medical affairs activities comply with relevant codes of practice and regulatory requirements.
• Provide medical oversight for pharmacovigilance and contribute to risk mitigation.