Medical Affairs Manager Specialty

GSK • New York, NY

4d • Hybrid

About The Position

You will lead local medical activities for specialty therapy areas in the Philippines. You will work closely with cross-functional teams and external healthcare experts. We value collaborators who bring scientific rigour, clear communication, and a passion for improving patient outcomes. You will have room to grow, shape medical strategy, and contribute to our mission of uniting science, technology and talent to get ahead of disease together. This role will provide YOU the opportunity to lead key activities to progress YOUR career.

Requirements

• Medical Doctor, Pharmacist, or MSc/PhD in Life Sciences.
• Minimum 3 years’ experience in Medical Affairs or a related role in the pharmaceutical industry.
• Experience engaging with healthcare professionals and key external experts.
• Proven ability to deliver medical education, advisory boards, or scientific meetings.
• Strong written and verbal communication skills in English.
• Ability to work effectively in cross-functional teams and manage multiple priorities.

Nice To Haves

• Experience in specialty therapeutic areas such as respiratory, immunology, or related fields.
• Experience in clinical research, protocol development, or study management.
• Familiarity with medical governance, regulatory, and pharmacovigilance processes.
• Project management skills and experience managing budgets.
• Prior experience working in the Philippines healthcare environment.
• Additional language skills relevant to local markets.

Responsibilities

• Develop and implement local medical strategies and customer engagement plans for assigned specialty therapy areas.
• Build and maintain trusted relationships with healthcare professionals and external clinical experts.
• Lead medical education activities, advisory boards, and scientific exchanges aligned with medical governance.
• Support clinical research and evidence generation activities, including observational studies and post‑marketing research.
• Review and approve scientific, promotional and non‑promotional materials to ensure accuracy and compliance.
• Provide medical input to cross-functional teams for launch planning, lifecycle management, and reimbursement discussions.

Benefits

• You will join a team focused on scientific excellence and patient impact.
• You will get practical opportunities to grow your skills and lead projects.
• You will work in a supportive environment that values inclusion and different perspectives.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Ph.D. or professional degree
• Number of Employees: 5,001-10,000 employees