Global Medical Director Cardiometabolic

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 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. #J-18808-Ljbffr