- Contribute to the development and execution of the global medical affairs strategy for maridebart cafraglutide.
- Serve as the Medical Affairs Representative on various global strategic teams.
- Capture clinical/scientific insights across all key markets and translate them into concrete strategies.
- Facilitate scientific engagements across a broad range of partners (e.g. Align and implement strategy for medical communications and related activities.
- Develop medical strategic plans and ensure consistent execution of outputs through Medical Affairs Teams.
- Provide strategic direction for study design and execution for medical affairs and other global studies.
- Enable access to medicines through clear understanding and education of treatment value.
- Determine resource and budget allocation necessary to deliver on medical strategies.
- Lead/support relationships with the external healthcare community.
- Serve as a medical representative in leadership, governance, and cross-functional teams.
- Support evidence generation that shapes the therapeutic area and informs the practice of medicine.
- Synthesize and integrate insights to deliver medical inputs into cross-regional/functional strategies.
- Review, approve, and ensure dissemination of medical communications and related activities.
- Compliance and Performance:
- Use global infrastructure for tracking, measuring, and evaluating performance and ensuring continuous performance improvement.
- MD plus accredited fellowship in Cardiology, Endocrinology, Obesity, Internal Medicine or related medical field. Minimum 5 years of Medical Affairs experience in industry (biotech, pharmaceutical or CRO)
- Experience in building Integrated Evidence Generation Plans
- Familiarity with global regulatory organizations, guidelines, and practices
- Knowledge of pharmaceutical product development, product lifecycle, and commercialization processes, including but not limited to, clinical operations, commercial, regulatory, and medical affairs
- History of solving problems while exhibiting sound scientific/medical judgment and a balanced, realistic understanding of issues
- Good understanding of healthcare systems around the world (e.g. As we work to develop treatments that take care of others, we also work to care for our teammates professional and personal growth and well-being.
- Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-winning time-off plans and bi-annual company-wide shutdowns
- Flexible work models, including remote work arrangements, where possible
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Medical Director, Global Asset Lead Obesity and Cardio-Metabolism - Washington DC, United States - Amgen
Description
It is key to our becoming one of the worlds leading biotechnology companies. We are global collaborators who achieve togetherresearching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide.Medical Director, Global Asset Lead, Obesity and Cardio-Metabolism, US- Remote****In this vital role the Global Asset Lead Medical Director will be accountable for the development and execution of global medical affairs strategy for Obesity and Cardio-Metabolism.
Strategy Development and Implementation:
Masters degree and 7 years of medical affairs or clinical development experience in obesity and/or cardio-metabolism
Bachelors degree and 9 years of medical affairs or clinical development experience in obesity and/or cardio-metabolism
**3 years of clinical research and/or medical affairs experience in a leadership role
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.
