Global Medical Director – Cardiometabolic
Abbott | Established Pharmaceutical Division
About Abbott
At Abbott, we believe people live their fullest lives when they are healthy — physically, emotionally, and socially. As a global healthcare leader with more than 107,000 colleagues across 160+ countries, we develop life‑changing medicines and technologies that support health at every stage of life.
Within our Branded Generics business, we make trusted, high‑quality medicines accessible to more than 18 million people every day, particularly in fast‑growing regions such as LATAM, APAC, India, and Emerging Markets. Our diverse portfolio spans critical therapeutic areas including Women’s Health, Gastroenterology, Cardiometabolic, CNS & Pain, and Respiratory, addressing real and often unmet patient needs worldwide.
Abbott is a place where science, purpose, and people come together — and where diverse perspectives, inclusive leadership, and collaboration are essential to building better outcomes for patients.
Your Impact
As Global Medical Director – Cardiometabolic, you will play a pivotal role in shaping Abbott’s global medical strategy for the Cardiometabolic therapeutic area. Working as a trusted partner across functions, you will help define both short‑ and long‑term direction, ensuring that medical decision‑making remains scientifically rigorous, patient‑focused, and globally aligned.
You will be a core member of the Medical Affairs Leadership Team within the Established Pharmaceuticals Division (EPD), contributing your expertise and perspective to key strategic decisions across Medical Affairs, Innovation & Development.
What You Will Do
Medical Strategy & Scientific Leadership
Lead the global medical strategy and activities for the Cardiometabolic therapeutic area and assigned products
Collaborate closely with cross‑functional partners to translate scientific insight into meaningful medical and patient impact
Identify unmet medical needs and mid‑ to long‑term opportunities for differentiation, innovation, and value creation
Continuously evaluate products within scope, identifying portfolio gap‑filling opportunities, including in‑licensing considerations
Develop therapeutic area medical plans, integrating research priorities, publication strategies, real‑world evidence, and study initiatives
Prepare Target Product Profiles (TPPs) in partnership with cross‑functional teams
Evidence Generation & Governance
Lead and govern Global Medical Affairs research projects, including IIS, post‑marketing studies, observational and epidemiologic research, Phase IV and RWE studies
Serve as Chair of the Scientific Review Committee for GMA‑led clinical research activities
Jointly review and approve clinical activities led by Clinical Development teams
Drive high‑quality scientific content for digital initiatives aimed at both HCPs and patients
Collaboration, Safety & Compliance
Build and sustain strong collaboration with regional and local Medical Directors, ensuring alignment between global strategy and local execution
Establish and maintain trusted, ethical relationships with Key Opinion Leaders and scientific societies
Act as a core member of the Product Safety Team, overseeing medical safety monitoring and contributing to PSURs, clinical overviews, and risk management plans
As part of the Labeling Sub‑Team, provide medical input and scientific strategies for global and national label changes, including safety‑related updates
Ensure that all medical and promotional activities comply with global guidelines and regulatory requirements
People Leadership
Lead and develop one direct report, fostering a collaborative, inclusive, and high‑performing environment
Attract, mentor, and retain talent through servant leadership, coaching, and empowerment
Support a culture where diverse voices are encouraged and valued
What We’re Looking For
Education & Experience
Advanced degree in Life Sciences, such as:
M.D. (preferred) with 5+ years of relevant pharmaceutical experience
PharmD / PhD with 7+ years of experience
M.Sc. with 10+ years of experience in the pharmaceutical industry
Strong experience in Medical Affairs and/or clinical research, in pharma, academia, or equivalent settings
Solid understanding of clinical trial methodology, safety oversight, and regulatory requirements
Proven experience engaging Key Opinion Leaders and scientific societies
Leadership & Skills
Fluency in English (written and spoken); additional languages are an asset
Experience in country or regional medical roles is desirable
Demonstrated servant leadership and ability to influence in complex, matrix environments
Strong communication, presentation, and stakeholder‑engagement skills
Sound business acumen within the pharmaceutical industry
Comfort operating in strategic roles with accountability and shared ownership
We encourage applications even if you do not meet every criterion.
Many successful leaders grow into roles through experience, perspective, and motivation — not by matching every requirement on paper.
Why Abbott
Purpose‑driven work that improves access to healthcare globally
A culture that values diversity, inclusion, empathy, and thoughtful leadership
Opportunities for international collaboration and long‑term career growth
An environment where your expertise, voice, and perspective truly matter
Abbott is proud to be an Equal Opportunity Employer, committed to building teams that reflect the patients and communities we serve.
Ready to Join Us?
If this opportunity resonates with you — even if you are unsure you meet every requirement — we’d love to learn more about you.
Please submit your CV as a PDF via our careers site.
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