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- Lead to the development of strategic and aligned Medical Affairs Plans for your assigned therapeutic area and communicate these plans to upper/senior management
- Direct, design and strategize the planning and implementation of late-phase clinical studies
- Provide medical oversight for protocol development, trial results, and final reports and publications.
- Serve as study director for trials.
- Be the medical/Scientific subject matter. This relates to the following activities; CRC, scientific communications, publication planning/review, advisory boards, health outcomes plans, MSL activities, speaker programs, investigator-initiated research, etc.
- External leadership: Provides leadership and strategic direction to stakeholders as well as external customers, and other key relationships within the business.
- Participate actively in external events and activities.
- PhD within Neurosciences, or a related field of science. (Medical Doctor Degree preferred)
- Proven experience in driving successful medical affairs strategies.
- Experience in medical affairs activities for Neurology products, specifically, Alzheimers
- Clinical research experience, including conducting clinical trials in the Phase IIIb-IV area.
- Up-to-date knowledge of the Neurology product area and pharmaceutical landscapes.
- Competitive salary and performance-based bonus
- Comprehensive health, dental, and vision insurance
- Generous paid time off and flexible work hours
- Continuous development through mentorship and training programs
Medical Affairs Director Neurodegeneration - New Jersey, United States - Leaman Life Sciences
Description
This is a new exciting opportunity to work for a global pharmaceutical company that is making significant progress and changes for patients worldwide who suffer from diseases related to Neurology.
This role is for a Medical Director, a strategic role where you have control and oversight of medical affairs activities for Neurodegenerative disease products.
Responsibilities:
Requirements:
Benefits: