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Senior Program Director (Commercial Regulatory Affairs, Fully Remote)

Dawar Consulting, Inc.
Posted 2 months ago, valid for 16 days
Location

South San Francisco, CA 94080, US

Salary

$120 - $127 per hour

Contract type

Contract

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Sonic Summary

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  • Our client, a leading biotechnology and life sciences company, is hiring a Senior Program Director for Commercial Regulatory Affairs in South San Francisco, CA, with a fully remote option.
  • This long-term contract position pays between $120 and $127 per hour on a W2 basis, along with comprehensive company benefits including medical, dental, vision, paid sick leave, and a 401K plan.
  • The role requires a minimum of 7 years of experience in Regulatory Affairs, Commercial Regulatory, Compliance, or Advertising & Promotion within the biotech or pharmaceutical industry.
  • Key responsibilities include leading Promotional Review Committees, reviewing promotional materials, and ensuring compliance with FDA regulations while collaborating with various internal teams.
  • Candidates should possess a Bachelor's degree, with advanced degrees preferred, and demonstrate strong communication and leadership skills in a fast-paced environment.
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 hr@dawarconsulting.com/lakshmi@dawarconsulting.com




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