Acadia Pharmaceuticals Inc. logo

Director Scientific, Communication & Medical Information Int'l Partnership

Acadia Pharmaceuticals Inc.
Full-time
Remote friendly (San Diego, CA)
United States
$187,000 - $233,900 USD yearly
Medical Affairs

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Role Summary

The Director will serve as Medical Affairs primary point of contact for international partnerships (Named Patient Sales program) outside North America and Europe for Acadia products, focusing on rare diseases. The role involves managing Medical Affairs initiatives of the international NPS program, sharing appropriate medical content for scientific exchange, and responding to escalated Medical Information inquiries. It requires strategic and operational input as a cross-functional interface between Acadia headquarters and partner markets.

Responsibilities

  • Manages Medical Affairs initiatives with partners of the international NPS program; ensuring Medical strategies are shared and discussed for alignment
  • Works across matrix teams and regions to ensure relevant insights are considered for overall strategy development
  • Coordinates with Learning & Development on training needs (onboarding as well as continued training as new data becomes available)
  • Maintains and coordinates transfer of appropriate Medical Content for scientific exchange and for responding to Med Info inquiries for international partnerships
  • Manages escalated Med Info inquiries from partner markets and ensures accurate and timely responses
  • Coordinates with Medical Affairs colleagues and internal stakeholders in the development, review and approval of Medical Content for partner markets, as needed
  • Maintains understanding of product knowledge and labeling, associated disease states, relevant literature, treatment guidelines, competitor information, and marketing strategies and tactics for assigned therapeutic area(s)
  • Acts as a subject matter expert to the partners to provide timely up-to-date scientific and clinical information necessary to make impactful business decisions
  • Contributes to the development, review and implementation of long and short-term strategies to optimize assigned partner markets for future and current products
  • Develops and maintains a strong working relationship with the partners, ensuring alignment with program objectives, timelines, and quality standards aligned to global and medical affairs strategy
  • Collaborates with local, regional and global cross-functional teams to address program requirements and challenges
  • Collaborates learnings and best practices with leadership, headquarters and with partners
  • Other responsibilities as assigned

Qualifications

  • Requires a PharmD, PhD, or MD degree in a scientific discipline. Targeting 7 years of Medical Affairs experience in pharmaceutical/biotech, with 5 years in Medical Affairs/Scientific Communications/Medical Information. An equivalent combination of education and experience may be considered.
  • International experience within Medical Affairs/Sci Com/Med Info is preferred.
  • Experience with rare disease/neurology is preferred.
  • Ability to work across multiple functions, geographies and business cultures.
  • Experience in literature searches, literature evaluation, and drug information concepts.
  • Experience in developing medical content for scientific exchange and in response to Medical Information requests.
  • Experience in MLR and MRC.
  • Strong analytical and problem-solving skills.
  • Understanding of the legal and regulatory environment of pharmaceutical industry desired.
  • Thinks and acts with urgency while considering the broader impact on the organization
  • Confidently executes on and communicates decisions and rationale.
  • Anticipates risk and implements strategies to avoid potential problems. When appropriate, elevates to supervisor and other appropriate functional leaders as needed.
  • Ability to travel, including international travel.

Skills

  • Strategic cross-functional collaboration
  • Medical content development for scientific exchange
  • Medical Information and medical content management
  • Regulatory and compliance awareness
  • Data analysis and strategic planning

Education

  • PharmD, PhD, or MD degree in a scientific discipline

Additional Requirements

  • Ability to travel, including international travel
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