Associate Director, Medical Affairs

Job Description

Associate Director Medical Affairs

Job Description

Join our dynamic and inclusive organisation as the Therapeutic Area (TA) Lead of our industry-leading medical affairs team. Here you will hold the overall responsibility for developing executing and delivering tactical objectives outlined in our Medical Affairs Plans for the assigned therapeutic areas in India. You will lead an medical affairs team and work in collaboration with your Cross-functional counterparts to provide expert strategic input in support of the objectives of the therapeutic area. Your expertise and healthcare professional-focused approach will be vital in developing professional relationships with scientific and clinical leaders in. Youll work closely with other TA Leads as part of the India Medical Leadership Team ensuring alignment with our overall strategic objectives. Additionally you will engage with regulatory bodies payer groups and key advocacy organizations to further drive our efforts.

This role presents an incredible opportunity to partner with the Asia Pacific Global Medical Affairs sharing your medical and scientific expertise with counterparts in the region. You will also collaborate with functional teams such as Regulatory Affairs Legal GCTO and Marketing. With your guidance our team will maintain operational and fiscal excellence in the medical affairs directorate ensuring the utmost level of quality and compliance.

Primary Responsibilities :

• Lead the designated Team in the development of Medical Affairs plans (and associated metrics). Ensure that the plan is executed on time and to a high standard.
• Build and maintain strategic partnerships with key opinion leaders academic institutions and external collaborators. Represent the company in scientific and medical forums establishing a strong presence in the community.
• Model and manage for inclusive and collaborative leadership cross-functionally ensuring excellent partnership with the RDMA (Regional Director Medical Affairs) Global Clinical Trial Operations (GCTO) Global Clinical Scientific Affairs (GCSA) Pharmacovigilance (PV) and relevant sub-teams at regional / country level.
• Provides input structure and oversight to the local data generation process partnering with CORE in outcomes research with GCD in company-sponsored interventional studies and with Global Center for Scientific Affairs (GCSA) on areas of interest for the investigator-initiated study program.
• Work in close partnership with Human Health (commercial) colleagues to ensure appropriate strategic alignment.
• Use innovative approaches to translate these Medical Affairs plans into research data analysis scientific communication educational and other solutions that inform clinical practice improve patient outcomes and enhance access.
• Communicate both scientific needs credibly and effectively across a variety of internal and external stakeholders at all levels.
• Demonstrate influence in external scientific community be it through peer-to-peer interactions research and educational collaborations publications or other
• Participate in and contribute significantly to professional organizations academic or regulatory working teams.
• Successfully collaborate and provide medical input into regulatory policy compliance and other issues management.
• Planning and execution of GMSA congress activities including training scientific leader interactions communicating results and insight generation.
• Lead talent review process and demonstrate follow through on Development Plans. Create action plans to ensure effective succession pools for leadershippositions within the team.
• Play a key role in the Country Medical leadership team.

Education :

Required Experience and Skills :

Preferred Experience and Skills :

We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we follow the science that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe.

We are proud to be a company that embraces the value of bringing diverse talented and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one anothers thinking and approach problems collectively. We are an equal opportunity employer committed to fostering an inclusive and diverse workplace.

Required Skills :

Clinical Medicine Interventional Oncology Oncology

Preferred Skills :

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Merck & Co. Inc. Rahway NJ USA also known as Merck Sharp & Dohme LLC Rahway NJ USA does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place introductions are position specific. Please no phone calls or emails.

Employee Status : Regular

Relocation : VISA Sponsorship :

Travel Requirements :

Flexible Work Arrangements :

Not Applicable

Shift :

Valid Driving License :

Hazardous Material(s) :

Job Posting End Date :

12 / 16 / 2025

Required Experience :

Director

Key Skills

EMR Systems,Post Residency Experience,Occupational Health Experience,Clinical Research,Managed Care,Primary Care Experience,Medical Management,Utilization Management,Clinical Development,Clinical Trials,Leadership Experience,Medicare

Employment Type : Full-Time

Experience : years

Vacancy : 1