Develop and refine clear, compelling scientific messaging across programs and stages of development
Draft and manage scientific content such as slide decks, congress materials, medical Information letters, medical affairs and training materials, FAQs and background documents, and external sci comm projects (e.g. webinars, podcast, product theaters, symposia)
Translate preclinical, translational, and clinical data into audience-appropriate communications
Partner cross-functionally with Medical Affairs, Clinical Development, Regulatory, and company leadership to ensure scientific accuracy and message consistency
Help prepare materials for advisory boards, investigator meetings, and scientific congresses
Contribute to the development of the company’s scientific narrative as programs advance
Help build and maintain core Medical Information content and processes in an early-stage company environment
Develop, review, and update standard medical response documents and reference materials
Research and synthesize literature and internal data to support responses to unsolicited medical inquiries
Ensure responses are accurate, balanced, evidence-based, and compliant with internal and external requirements
Partner with Medical Affairs, Regulatory, and Pharmacovigilance to support appropriate documentation and escalation of medical inquiries, adverse events, and product complaints, as applicable
Maintain a library of response letters, FAQs, and scientific references
Identify trends in incoming medical questions and share insights with internal stakeholders
Support training of internal teams on scientific messaging and Medical Information processes
Help manage external Medical Information vendors or agency partners, when applicable
Requirements
Advanced degree in life sciences preferred
Approximately 5+ years of relevant experience in scientific communications, medical communications, medical affairs, medical information, or a related biotech/pharma function
Experience in dermatology or immunology strongly preferred
Strong scientific writing and editing skills, with the ability to tailor content to different audiences
Solid understanding of drug development, clinical research, and interpretation of scientific data
Experience supporting scientific communications deliverables such as presentations and congress materials
Experience developing or reviewing Medical Information content is strongly preferred
Strong attention to detail and commitment to scientific accuracy and compliance
Able to work independently, manage multiple priorities, and adapt quickly in a startup setting
Experience working with vendors, medical writers, or outsourced contact center/Med Info partners
Collaborative, practical, and comfortable working across functions with limited structure.
Benefits
A chance to be part of a vibrant startup culture where your work can directly impact bringing new medicines to patients.
Competitive salary and benefits package.
A supportive and inclusive team environment where everyone is encouraged to bring their authentic selves to work.
Opportunities for professional growth and development.