Overview
Develop high-quality scientific content that supports strategic communication initiatives for pharmaceutical and biotech clients across a variety of therapeutic areas.
What you'll do
- Develop scientific content such as slide decks, executive summaries and meeting materials that is client-ready and scientifically rigorous.
- Collaborate with cross-functional teams, including 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 all 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.
- Eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, 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.