Associate Director, Regulatory Affairs, Advertising, Promotion & Labeling
Kyverna · United States · US
Regulatory Affairs
Remote
physician
Pharmacist
Demand78
Career growth72
Healthcare fit58
Remote potential85
Salary band
USD 180k – 205k
5-year outlook
Senior biopharma regulatory roles generally remain competitive and well compensated, especially with advertising/promotion and labeling expertise. Exact pay and progression will vary by company stage, location, launch record, and scope of FDA/OPDP experience.
Clinical license
Not required
Applicant reach
narrow
Seniority
senior
Employment type
full-time
Date found
2026-10-27
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Eligible countries
- United States
- Profession fit
- physician, Pharmacist
- 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 considering only if you already have substantial biopharma regulatory, promotional review, MLR, labeling, or OPDP experience. It is not a realistic entry point for clinicians without a prior regulatory or medical affairs track.
Who should apply
Physicians, pharmacists, or IMGs with biopharma regulatory affairs experience, especially in advertising/promotion, promotional review, MLR, labeling, USPI, OPDP interactions, product launch, or lifecycle management.
CV angle
Frame real regulatory, medical affairs, or promotional review experience around FDA/OPDP interactions, MLR committee leadership, USPI/labeling strategy, launch and lifecycle support, SOP/process improvement, cross-functional work with Commercial/Medical/Legal/Compliance, and Veeva PromoMats. Clinicians without direct regulatory experience should emphasize evidence review, guideline interpretation, quality/compliance, committee leadership, and scientific communication without claiming regulatory roles they have not held.
Skills to highlight
- FDA promotional regulations
- Advertising and promotion review
- US Prescribing Information (USPI) and labeling
- OPDP/APLB interactions
- Medical/legal/regulatory (MLR) review
- Cross-functional leadership
- Veeva PromoMats
- Regulatory SOP/process improvement
Role summary
Senior regulatory affairs role leading US promotional, advertising, and labeling strategy for a biopharma company, including FDA OPDP interactions, MLR review, labeling negotiations, process improvement, and cross-functional commercialization support.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.