Medical Affairs Manager Oncology

Job Description

Industry: Biotechnology Research, Pharmaceutical Manufacturing, and Veterinary Services
Seniority for this role: Not Applicable
Job Description We are seeking a highly skilled and motivated Medical Affairs Manager (MAM) to join our dynamic team. Under the general supervision of the Medical Director/Therapeutic Area Lead, the MAM will be responsible for managing medical activities within one or more therapeutic areas. The MAM will collaborate with marketing, market access, and other cross-functional teams to drive strategic medical initiatives that align with business objectives and enhance the overall product lifecycle. This role offers a unique opportunity to lead high-level scientific interactions, contribute to business strategies, and support market access and health economics efforts while ensuring compliance with local regulations and policies. Key Responsibilities Strategic Planning & Implementation Contribute to short and long-term business objectives by driving medical and clinical excellence throughout the product lifecycle within the therapeutic area. Develop and implement the Country Medical Affairs Plan (CMAP) to ensure the successful delivery of medical affairs activities. Collaborate with cross-functional teams to align medical strategies with brand imperatives, market access objectives, and clinical needs. Represent the company in external structures, including Advisory Boards, Expert Input Forums, and regional task forces. Scientific & Medical Interactions Manage and maintain high-level scientific and clinical interactions with Scientific Leaders, investigators, speakers, and scientific societies. Conduct over 50% of the role through customer interactions via meetings, emails, phone calls, and congresses/symposia. Provide medical and scientific advice to internal teams and key stakeholders, ensuring scientific accuracy and compliance with regulations. Lead the planning and execution of national and regional Advisory Boards, contributing to formulary and clinical guideline development. Clinical Activities & Publications Lead the management and execution of Global Medical Affairs (GMA) programs, local studies, and clinical evaluations, ensuring adherence to timelines and budgets. Secure input for HQ-sponsored studies and manage national site selection. Implement publication policies, ensuring the timely publication of review articles and scientific manuscripts. Identify and explore opportunities for relevant medical meetings, CME programs, and research grants that bring value to the therapeutic area. Internal Collaboration Provide medical and scientific expertise and training to internal teams, offering support and advice within the therapeutic area. Work closely with Market Access teams to ensure the successful implementation of pricing, reimbursement, and access strategies. Collaborate with Regulatory Affairs to ensure accuracy in labeling, safety information, and compliance. Ensure clinical and scientific accuracy of promotional materials through the worldwide review process. Required Skills & Qualifications Medical Degree (MD), PhD, or PharmaD in life sciences (preferred). Relevant prior experience in a similar role, preferably in Oncology or other therapeutic areas. In-depth knowledge of the drug development process and local medical practice. Strong ethics, integrity, and leadership capabilities. Excellent interpersonal and communication skills, with the ability to manage relationships with scientific leaders and authorities. Proven ability to collaborate within a matrix organization and problem-solve effectively. Proficiency in English and strong presentation skills. Ability to manage multiple projects simultaneously and work effectively across teams. What We Offer Opportunity to work with a dynamic team on cutting-edge medical innovations. Competitive salary and benefits package. A collaborative and innovative work environment. Career development opportunities in a global organization. If you are passionate about making an impact in the medical field and driving excellence in therapeutic areas, we would love to hear from you! Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully 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 Domestic VISA Sponsorship No Travel Requirements 25% Flexible Work Arrangements Not Applicable Shift Not Indicated Valid Driving License No Hazardous Material(s) n/a Job Posting End Date 01/22/2025 A job posting is effective until 11 59 59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID R324063 Show more Show less