Associate Manager Scientific Writing
Regeneron · United States · US
Medical Writing
Remote
Pharmacist
Dentist
Demand80
Career growth75
Healthcare fit82
Remote potential100
Salary band
USD 110k – 179k
5-year outlook
Pharma scientific and regulatory writing compensation is generally stable to growing, with progression into senior writing or management. Exact pay depends on country, degree, and experience; no figures are stated in the posting.
Clinical license
Not required
Applicant reach
moderate
Seniority
mid
Employment type
full-time
Date found
2026-10-02
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Eligible countries
- United States
- Profession fit
- Pharmacist, 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
Worth applying if you have regulatory or medical writing experience in pharma and want a remote scientific writing leadership track. Clinicians without industry writing experience are unlikely to be competitive.
Who should apply
PharmDs, PhDs, MDs, and IMGs with 3+ years of pharma regulatory writing or medical writing experience, especially those who have coordinated documents, cross-functional teams, or author training.
CV angle
Reframe clinical and research experience as regulatory/scientific writing: highlight protocols, investigator brochures, CSRs, publications, SOP/template development, cross-functional drug development teams, timeline/resource coordination, and mentoring. Use ATS terms like regulatory documents, scientific writing, project management, and cross-functional collaboration.
Skills to highlight
- Regulatory writing
- Scientific writing
- Project management
- Cross-functional collaboration
- SOP and template development
- Training and mentoring
- Process improvement
- Microsoft Office/Adobe Acrobat/AI tools
Role summary
Coordinate and support regulatory document authors across disciplines, manage timelines and resources, monitor document quality and process adherence, and contribute to training and process improvement within a pharma scientific writing group.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.