YOUR TASKS AND RESPONSIBILITIES

The primary responsibilities of this role, Director Medical Affairs MD -Women's Health, are to: 

• Active participation and effective interaction with US and Global teams to ensure appropriate direction of the company’s research and marketing efforts relative to the US environment as well as responsible for the execution of an overall medical strategy:

• Provide support and medical expertise to US cross-functional teams within the Business Unit regarding development of educational materials, monitoring of published literature, addressing and resolving international, regional and local issues related to products under their responsibility and provide input to company documents to ensure scientific accuracy as well as implement the Medical Affairs Brand Plan,communication and publication programs with approved budgets:

• Support completion of annual NDA reports for respective brands through evaluation of clinical data and literature and provide USMA input in the preparation of key medical documents for INDs and NDAs. This includes ensuring appropriate USMA input in interactions with the FDA:

• Participate in scientific review of investigator initiated studies and be answerable medically for the clinical studies under their direction as well as directing the design, conduct, analysis and reporting of Phase IV US clinical trials:

• Participate in the Grant Review and Advisory Committees:

• Explore and evaluate new product ideas to assist in identifying new marketing opportunities and perform medical evaluations and due diligence on pharmaceutical products for in-licensing in the US:

• Interface with both internal and external (KOLs, advisors, consultants) experts and medical organizations in order to develop and maintain productive contacts:

• Collaborator with other members of the team as well as internal and external personnel:

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WHO YOU ARE

Your success will be driven by your demonstration of our LIFE values.  More specifically related to this position, Bayer seeks an incumbent who possesses the following:

Required Qualifications:

• M.D. Degree or equivalent:
• 2+ years of clinically relevant or independent research experience or equivalent OR 2+ years’ experience in the pharmaceutical or related industry or of extensive collaboration with the industry (eg,lead PI and consultant, FDA employee or advisor):
• Proven ability to identify and resolve complex problems:
• A solid understanding of clinical study design, analysis and interpretation as well as the principles of observational studies and health economics:
• Ability to collaborate with a variety of teams and personnel as well as a proven ability to interact effectively with key opinion leaders:
• Highly developed ethics and integrity, with demonstrated ethical medical decision making skills:
• Ability to work well on teams:
• Proven ability to implement successful clinical strategies and programs:
• Effective communicator with strong oral and written communications skills.: