Senior Medical Affairs Physician (m/f/d)

YOUR TASKS AND RESPONSIBILITIES

• Provide senior medical expertise in cardiometabolic disease, and nephrology and insights on commercial issues through membership in cross-functional teams and task forces 
• Lead the creation, coordinate, and support the implementation of the strategic Medical Affairs Plan of Finerenone 
• Plan and conduct Scientific Advisory Boards with Thought Leaders (TLs) and External Customers & represent BAYER viewpoint on products to TLs, Scientific Advisors, Health Authorities and to other External Stakeholders 
• Provide Medical Affairs input to Global Clinical Development Programs, provide the Medical Strategy and Review for Global Phase IV Studies, Investigator Initiated Research & Real-World-Evidence analyses and ensures all regional studies are consistent with agreed Global Medical Strategy 
• Provide Medical Review of promotional material for Global Use (e.g., Product Monographs, Brochures, Press Releases, Q&As, and Field Communications)
• Contribute or lead Medical Affairs activity connected to the Scientific Publication Process, Global Thought Leaders Development Programs and Global Medical Congress Activity 
• Contribute or lead development of medical and scientific communication material and subsequently of global training programs (Speakers Trainings, MSL Training, and Marketing Training) and its implementation in regional Medical Affairs functions as well 
• Provide Medical Affairs input to Core Labeling and Pharmacovigilance documents for marketed products (e.g., risk management plans and benefit-analysis for risk-benefit assessments) 

WHO YOU ARE

• University degree in Medicine or equivalent (MD, PhD), preferrable with either a strong background in nephrology (e.g., residency in nephrology) or a strong expertise in the field of cardiometabolic disease or nephrology 
• Long-term experience in Clinical Development and/or Medical Affairs function of a Global Healthcare Organization or equivalent in Academic environment or Global, Regional or Country Pharmaceutical environment 
• Understanding of companion diagnostic development process desirable 
• Strong experience of developing and delivering medical information materials, presentations, and publications in English 
• Experience of effectively managing risk and compliance issues 
• Experience of participating in cross-functional teams and of working across and building effective working relationships between functions 
• Track record of successful project management and overall budget responsibility with a strong background in organizing scientific symposia, preparing, and leading advisory boards and collaborating with healthcare organizations 
• Highly effective communicator with good influencing ability and strong written and oral communication skills, high degree of fluency in written and verbal English required

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