MindMed is hiring a
Senior Director

Summary

The Senior Director, Global Medical Affairs will contribute to the development of a medical affairs strategy for MindMed's central nervous system (CNS) development portfolio. Responsibilities include understanding the science behind treatments, identifying clinical endpoints, engaging with key stakeholders, and developing strategies to engage external stakeholders. The role requires a M.D., Ph.D., or equivalent advanced scientific or clinical degree with 10+ years of experience in biotechnology or pharmaceutical industry.

Requirements

• M.D., Ph.D., or equivalent advanced scientific or clinical degree (Pharm.D., Psy.D.)
• 10+ years of progressive experience in biotechnology or pharmaceutical industry, with increasing leadership responsibilities and accountabilities in a Medical Affairs role

Responsibilities

• Help the Vice President of Global Medical Affairs build and oversee a capable and talented Global Medical Affairs organization
• Contribute to medical affairs activities such as strategic insight gathering/exchange, strategic publication planning, development and conduct of medical/scientific advisory boards and educational programs, response to requests for scientific/medical information, and scientific/medical interaction with healthcare providers, thought leaders, payers and other key external stakeholders
• Develop and deliver accurate and fair-balanced clinical/scientific information to healthcare professionals in accordance with promotional compliance and regulatory requirements
• Represent Mindmed’s science externally with the highest standards of evidentiary rigor and scientific credibility
• Engage with patient advocacy groups to exchange scientific/medical knowledge and enable patient engagement and input into planning and execution of clinical trials, and into commercial planning
• Actively contribute to strategic project plans, including but not limited to integrated product strategy, integrated evidence plan, scientific/medical communication plans, patient advocacy engagement plans, future launch planning, and other key program deliverables across the product lifecycle
• Help select and manage external scientific communication and patient engagement partners
• May lead, manage and coach a team of medical affairs professionals, including medical directors, medical science liaisons and other relevant staff

Benefits

• Work is performed primarily in a remote office environment with occasional in-person meetings, and/or travel
• Less than 25% travel at this time, and it may increase depending on the needs