Senior Director, Medical Writing – Biologics
SAB Biotherapeutics · United States · US
Medical Writing
Remote
physician
Pharmacist
Nurse
Demand85
Career growth75
Healthcare fit55
Remote potential70
Salary band
USD 190k – 260k
5-year outlook
Senior Director-level medical writing roles in biologics typically command high compensation and remain in demand as regulatory complexity grows; exact salary depends on location, company stage, and equity.
Clinical license
Not required
Applicant reach
narrow
Seniority
executive
Employment type
full-time
Date found
2026-10-06
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Eligible countries
- United States
- License jurisdiction
- US
- Profession fit
- physician, Pharmacist, Nurse
- 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
Only consider if you have 12+ years of medical writing experience and hands-on BLA/MAA leadership; clinicians without a regulatory writing track record are unlikely to be competitive.
Who should apply
Senior medical writers with biologics and immunology experience, especially MD/PharmD/PhD professionals who have led FDA/EMA submissions.
CV angle
Frame clinical and research experience around regulatory document authorship, BLA/MAA/CSR contributions, cross-functional leadership, and compliance with ICH/GCP/FDA/EMA; quantify submission milestones and therapeutic area depth.
Skills to highlight
- Medical Writing
- Regulatory Submissions
- BLA/MAA
- eCTD/CTD
- ICH/GCP
- Cross-Functional Collaboration
- Biologics/Immunology
- Project Management
Role summary
Lead end-to-end medical writing for biologic products, authoring and managing regulatory documents such as BLAs, MAAs, CSRs, ISS/ISE, and responses to health authorities.
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