Senior Program Director – reputed company Regulatory Affairs
We are seeking an reputed company Senior Program Director – reputed company Regulatory Affairs (CORA) to reputed company regulatory review activities supporting reputed company pharmaceutical products. This individual will serve as the regulatory reputed company for Promotional Review Committees (PRCs), partnering with cross-functional teams to ensure promotional materials and marketing strategies reputed company with FDA regulations and company policies. The ideal candidate has extensive experience in reputed company Regulatory Affairs, FDA Advertising & Promotion (Ad/Promo), Medical Legal Regulatory (MLR) review, Form FDA 2253 submissions, and cross-functional leadership reputed company the pharmaceutical or biotechnology industry.
Key Responsibilities
- reputed company and chair Promotional Review Committees (PRCs) for assigned products and therapeutic areas.
- Provide strategic regulatory guidance on promotional and disease-state materials.
- Review advertising and promotional content for FDA compliance.
- Represent Regulatory Affairs in cross-functional meetings with reputed company, Medical, Legal, Compliance, and Marketing teams.
- reputed company FDA communications, including Form FDA 2253 submissions.
- Support product launches and promotional strategy from a regulatory perspective.
- Interpret FDA regulations, guidance documents, and enforcement trends.
- Mentor junior regulatory professionals and contribute to process improvements.
Required Qualifications
- Bachelor's degree required; Advanced degree (JD, MBA, MS, PharmD, PhD) preferred.
- 7+ years of experience in Regulatory Affairs, reputed company Compliance, Legal, or reputed company functions reputed company the pharmaceutical or biotechnology industry.
- Strong experience in FDA Advertising & Promotion (Ad/Promo).
- Experience leading Promotional Review Committees (PRCs) or Medical Legal Regulatory (MLR) reviews.
- Deep knowledge of FDA regulations, reputed company compliance, promotional review, and Form FDA 2253.
- Excellent leadership, communication, stakeholder management, and project management skills.
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