Scientific Narrative Lead
Praxis Precision Medicines · United States · US
Medical Affairs
Remote
physician
Dentist
Demand82
Career growth80
Healthcare fit80
Remote potential60
Salary band
USD 190k – 220k
5-year outlook
Likely competitive senior biopharma compensation with potential for director-level growth in medical affairs, regulatory strategy, or program leadership; exact figures depend on location, company stage, and equity.
Clinical license
Not required
Applicant reach
narrow
Seniority
lead
Employment type
full-time
Date found
2026-09-28
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Eligible countries
- United States
- Profession fit
- physician, Dentist
- Rate period
- Annual
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Strong fit for clinicians with biopharma, regulatory, or medical affairs experience who want a strategic non-clinical career. Clinicians without industry experience may find the 6+ year sponsor/CRO/consulting requirement a significant barrier.
Who should apply
Physicians, pharmacists, or advanced-degree clinicians with CNS, neuroscience, or rare disease backgrounds and experience in regulatory writing, medical affairs, clinical development, or scientific communications.
CV angle
Reframe clinical training as deep therapeutic and data fluency; highlight experience interpreting clinical evidence, contributing to protocols, CSRs, or regulatory documents, publication planning, and cross-functional collaboration. Emphasize ability to translate complex science into clear, consistent narratives for regulators, clinicians, and commercial partners.
Skills to highlight
- Scientific narrative development
- Regulatory submissions (IND/NDA/MAA)
- Medical writing and publications
- Cross-functional leadership
- CNS/neuroscience/rare disease expertise
- Clinical data interpretation
- Program strategy
- Stakeholder alignment
Role summary
Own the strategic scientific story for a lead development program, aligning regulatory submissions, publications, medical affairs, and commercial communications from clinical development through launch and lifecycle management.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.