About the position
Amylyx is looking for a Medical Affairs Manager who will providing support to the Medical Affairs to achieve short- and long-term medical objectives in alignment with the overall business strategy. This individual will be an integral member of the Amylyx Medical team, supporting ongoing and new medical initiatives including scientific exchange, medical education, publications, congress activities, advisory board meetings, medical information, and integrated evidence generation. The Manager will have the unique opportunity to be exposed to and gain experience in roles across the Medical Affairs function, taking on increasing responsibility in areas of interest over time. The role will report to the Director, Medical Affairs.
Responsibilities
- Collaborate with the Director of Medical Affairs to deliver key medical communications activities in assigned areas including, but not limited to: Publications, Scientific Platform, Advisory boards, Medical Information, Scientific Exchange Materials, Congress Planning, Promotional Material Review.
- Oversee and execute the strategic publication plan and scientific communications for congresses (abstracts, posters, oral presentations).
- Develop and continuously update scientific platform for assigned disease state(s).
- Support development of materials and content for advisory boards; ensure medical accuracy and appropriate review/approval and insight documentation.
- Lead the day-to-day operations of the in-house medical information function, including acting as a main point of contact to address requests, develop medical information content and ensure appropriate review/approval.
- Support the development and dissemination of scientific exchange materials, including reactive and proactive slide decks and print pieces.
- Partner with cross-functional congress planning team to ensure seamless execution of pre-, during, and post-congress activities.
- Provide timely and accurate reviews of promotional materials for assigned areas in accordance with established policies and practice standards, including regulatory guidelines to meet customer needs.
- Drive the successful completion of tactics supporting the Medical Affairs and Market Development Strategy for assigned programs, including literature reviews, data generation, lifecycle management, and HCP mapping.
Requirements
- Advanced scientific degree (PharmD, MD, or PhD).
- 2-3 years of clinical, scientific/research, or industry-related experience or equivalent.
- Knowledgeable of US and international regulations, requirements, and guidance associated with scientific publications.
- Experience supporting and/or leading research projects and publications processes.
- Ability to understand, critically analyze, and summarize complex scientific and medical data.
- Ability to work in fast paced, collaborative, cross-functional teams.
- Excellent planning and organizational skills.
- Excellent verbal/written communication, listening, and presentation skills.
- Proficiency in Microsoft Office platform and resources (i.e., Word, Excel, PowerPoint) and virtual platforms.
Nice-to-haves
- Basic knowledge of drug development process, clinical trial design, results and methodology, regulatory and compliance requirements.
- Preferred experience and knowledge in the following areas: rare disease, neurology, and/or endocrinology.
- Prior medical affairs, medical communications, publications and/or KOL management experience.
Benefits
- Remote work opportunities within the United States.
- Access to work in a setting which enables meeting all requirements of the role.
