Overview As an field-based Medical Science Liaison, you will be the scientific expert connecting clinicians and the company on Cushing's Syndrome, Cushing's Disease, and Acromegaly. You will foster peer-to-peer relationships with key opinion leaders and support unbiased scientific exchange. You'll translate complex data into meaningful medical content and support advisory boards, publications, and investigator-initiated studies. This role sits at the intersection of Medical Affairs and clinical development, helping to advance patient access and knowledge. You will work across cross-functional teams to educate and inform stakeholders while upholding compliance and high scientific standards.
Compensation / Benefits- Health insurance: medical, dental, vision, life and ADD
- 401k retirement benefits
- Paid time off (vacation, holidays, sick/personal)
- Annual performance bonus eligibility
Responsibilities- Deliver clinical and scientific presentations to clinicians, Endocrinologists, and P&T members
- Provide scientific support at medical conferences with up-to-date information on Cushing's Syndrome, Cushing's Disease, and Acromegaly for Isturisa, Signifor and Signifor LAR
- Maintain and expand peer-to-peer collaborations with key medical experts
- Respond to unsolicited medical information requests with a customized approach
- Collaborate on publications, investigator-initiated trials, and company-sponsored research
- Support clinical initiatives including site identification, registry work, and presentation of final data
- Provide medical input into the planning and execution of Advisory Boards and review speaker presentations
- Train staff (including sales) on key scientific topics
- Develop and review professional slide decks, medical letters, and clinical summaries
- Develop territory plan with input from manager and gather clinical field insights
- Understand and communicate the role of Medical Science Liaisons and Medical Affairs
- Ensure compliance with laws, regulations, and pharmacovigilance responsibilities
- Perform additional duties as assigned
Key requirements- Advanced scientific degree (M.D., D.O., Ph.D., Pharm.D.) in Medical, Biological Sciences
- Minimum of two years in Medical Affairs/Clinical functions (preferred)
- Familiarity with drug development, FDA, ICH, and GCP guidelines
- Experience in implementing or monitoring clinical trials is a plus
- Ability to review and interpret clinical data
- Ability to develop clinical data and medical content for presentations
- Proficiency in Microsoft Office (Word, PowerPoint, Excel)
- Strong presentation, written and verbal communication skills
- Independent work capability and good time management
- Strong presentation skills
- Excellent written and verbal communication
- Time management and independence
- Microsoft Office (Word, PowerPoint, Excel)
- Ability to interpret and synthesize clinical data
- Content development for medical presentations and letters
