Overview
Develop high-quality scientific content and communications for pharmaceutical and biotech clients across therapeutic areas, supporting the MLR review process.
What you'll do
- Develop scientifically rigorous, client-ready content such as slide decks, executive summaries and meeting materials.
- Collaborate with medical, editorial and client stakeholders to shape clear and compelling narratives.
- Support the medical/legal/regulatory (MLR) review process by addressing feedback, incorporating revisions and ensuring compliance with guidelines.
What you'll need
- Advanced scientific degree (PharmD, MD, or PhD).
- 2+ years of experience in a medical communications agency or similar environment.
- Strong experience developing scientific content across multiple formats (e.g., slide decks, publications, summaries).
- Demonstrated ability to conduct comprehensive literature searches and synthesize findings.
- Proficiency with Microsoft Word, PowerPoint, Excel, Adobe Acrobat, and reference management tools (e.g., EndNote).
- Experience participating in or supporting MLR review processes.
Nice to have
- Experience working with Medical Affairs and/or Publications deliverables.
- Exposure to commercial content development.
- Familiarity with multiple therapeutic areas or complex disease states.
Details
- Remote, United States.
- Reasonable estimated compensation range: $95,000 to $125,000 USD.
- Eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life and disability insurance, parental leave, and paid time off.
- Candidates must be legally authorized to work in the country of employment without employer sponsorship.
Read the full description and apply on the company’s own careers page.