Medical/Scientific Director, Medical Affairs- Psychiatry Pipeline

Job Description
*Preferred for this position to sit in our Lake County, IL orFlorham Park, NJ offices, but can be remote anywhere in the U.S.
*Position level will be determined by the qualifications listed below.
The Medical/Scientific Director, Medical Affairs - Psychiatry Pipeline is a strategic scientific expert with deep expertise across clinical, drug development, and medical strategy that acts as an influential leader within the R&
D organization to co-steward assets on cross-functional teams for assigned asset(s). The incumbent develops and executes medical strategy and tactics to secure insights, develop scientific value, advance pipeline assets, and provide strategic medical input to cross-functional partners. Responsible for core medical affairs activities including:
HCP and stakeholder interactions (prescribers/providers, KOL development, patient groups, payers), insight capture (advisory boards, real-world data analysis), generation and interpretation of clinical and scientific data, and educational initiatives (medical education, data, value proposition). Accountable for key medical affairs deliverables for assigned assets including comprehensive gap assessment, scientific communications platforms, scientific narratives, integrated evidence plans, and medical strategic plans.
Key Responsibilities:
Develop and execute medical affairs strategies and tactics
Work closely with cross-functional teams to ensure alignment of medical affairs strategies with overall business objectives.
Provide medical and scientific support to internal and external stakeholders, including key opinion leaders, clinicians, payers, and patients.
Build and maintain relationships with external stakeholders, including key opinion leaders, academic institutions, and regulatory agencies.
Lead the development and execution of scientific communication plans, including publication planning, medical education, and scientific exchange.
Provide input into clinical development plans, study protocols, and study reports to ensure alignment with medical affairs strategies.
Represent the company at scientific and medical conferences, symposia, and advisory boards.
Provide scientific and medical expertise to cross-functional teams, including research and development, regulatory affairs, market access, and commercial teams.
Ensure compliance with regulatory and ethical standards in all medical affairs activities.
Monitor and analyze market trends, competitor landscape, and regulatory changes to proactively identify potential challenges or opportunities for assets