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Dawar Consulting, Inc.

Senior Program Director (Commercial Regulatory Affairs, Fully Remote)

Remote — United States (see country and timezone requirements)

Check who can apply and the requirements below before continuing.

Job description

Our client, a world leader in biotechnology and life sciences, is seeking a "Senior Program Director, Commercial Regulatory Affairs".

Location: South San Francisco, CA (Fully Remote)

Duration:Long-Term Contract (Possibility Of Further Extension)

Pay Rate: $120-$127/hr on W2

Company Benefits: Medical, Dental, Vision, Paid Sick Leave, 401K

Job Summary

In this role, you will provide strategic regulatory guidance for U.S. commercial pharmaceutical products. You will lead Promotional Review Committees (PRCs), review and approve advertising and promotional materials, and partner closely with Marketing, Medical Affairs, Legal, and Compliance to ensure FDA‑compliant communications. This position offers the opportunity to shape commercial regulatory strategy for innovative therapies in a fast‑paced biotech environment.

Key Responsibilities:

Lead Promotional Review Committee (PRC) meetings

Review and approve promotional and marketing materials

Provide regulatory guidance on advertising and promotional claims

Partner with Marketing, Medical, Legal, and Compliance teams

Support FDA communications and Form 2253 submissions

Ensure compliance with FDA regulations and healthcare industry guidelines

Qualifications:

Bachelor's degree required; advanced degree (PharmD, PhD, JD, MBA, MS) preferred

7+ years of Regulatory Affairs, Commercial Regulatory, Compliance, or Advertising & Promotion experience in the biotech/pharmaceutical industry

Strong knowledge of FDA advertising & promotion regulations, promotional review, and healthcare compliance

Experience leading cross-functional teams and Promotional Review Committees (PRCs)

Excellent communication, stakeholder management, and project leadership skills

Preferred Skills:

Commercial Regulatory Affairs

Advertising & Promotion (Ad/Promo)

Promotional Review Committee (PRC)

FDA Form 2253

Medical, Legal, Regulatory (MLR) review

Product launch support

If interested, please share your updated resume at /

Originally posted on Himalayas

Who can apply

Eligible countries: United States. Accepted UTC offsets: UTC-10, UTC-9, UTC-8, UTC-7, UTC-6, UTC-5, UTC+14. Review the full description for employer-specific work authorization, residency and schedule requirements.

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