Full-Time Medical Director/Senior Medical Director
Glycomine is hiring a remote Full-Time Medical Director/Senior Medical Director. The career level for this job opening is Experienced and is accepting Boston, MA based applicants remotely. Read complete job description before applying.
Glycomine
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Overview:Glycomine is seeking a highly motivated and experienced Medical Director/Senior Medical Director, Medical Affairs to support development and pipeline efforts. This role acts as a scientific and clinical expert, bridging R&D, regulatory, and external stakeholders (e.g., healthcare providers, KOLs, and academic institutions). The candidate will provide expert medical and clinical insights to support pipeline development and launch readiness. Strong planning and execution of medical affairs strategies, and communication of complex scientific data are required. This role demands a collaborative and flexible approach in a fast-paced environment. Reports to the Chief Medical Officer.
Responsibilities:
- Develop and execute medical affairs plans aligned with product lifecycle stages.
- Support publications, abstracts, posters, and medical slide decks.
- Collaborate with Preclinical, Clinical Development, and Regulatory teams to translate clinical insights and data gaps into medical strategy.
- Provide medical leadership for therapeutic and disease area initiatives.
- Interact with investigators, KOLs, research institutions, and internal departments to oversee and facilitate Medical Affairs objectives.
- Build and maintain strong relationships with key opinion leaders, healthcare professionals, and academic institutions.
- Support short and long-term goals of Medical Affairs, prioritizing research interests and collaborations.
- Ensure alignment of Medical Affairs activities with launch readiness and program management plans.
- Provide medical review and approval of external resources, communication, and publications.
- Assist with planning and execution of advisory boards.
- Ensure all medical activities adhere to legal, regulatory, and corporate compliance standards.
- Represent the company at scientific and clinical congress meetings.
- Develop and deliver high-quality medical education and training materials.
- Lead efforts in developing patient registries and disease awareness campaigns.
Qualifications:
- MD with 5-10 years of medical affairs experience in the pharmaceutical or biotech industry.
- Prior experience in developing medical strategic and tactical plans.
- Deep understanding of clinical development, regulatory landscape, and scientific communications.
- Hands-on, collaborative, and solutions-oriented attitude.
- Excellent communication skills and proven ability to influence decisions.
- Willingness to travel and meet with HCPs/KOLs.
- Proven track record in leading medical strategy and supporting clinical development.
- Strong analytical and problem-solving skills.
- Ability to interact with senior management, academic experts, and patient advocates.