[Hiring] Senior Manager, Regulatory Affairs, Advertising and Promotion @SERVIER MONDE

Role Description

The Senior Manager, Regulatory Affairs Advertising and Promotion at Servier Pharmaceuticals will report to the Director of US Regulatory Affairs and Quality Management and is responsible for leading the day-to-day regulatory review of advertising, promotional, and educational materials. This role acts as a strategic partner to Marketing, Medical Affairs, and Legal, ensuring that company objectives are achieved through compliant and scientifically grounded messaging. You will contribute to the success of both marketed products and pipeline candidates as well as oversee submissions to the FDA Office of Prescription Drug Promotion (OPDP). This position offers a unique opportunity to help shape the regulatory framework of a growing, patient-centric organization.

Qualifications

• Bachelor’s degree in a scientific or healthcare field required
• 5+ years of professional experience in Regulatory Affairs, specifically within advertising and promotion in a biotech/pharmaceutical setting (Oncology and Rare Disease preferred)
• Strong expertise in FDA regulations and guidance documents
• Proficiency with electronic document management systems and promotional review platforms such as Veeva Vault
• Demonstrated ability to interpret complex clinical study reports and translate data into compliant promotional messaging and solutions
• Excellent interpersonal and influence skills to navigate cross-functional stakeholder requirements
• High level of organizational skills with the experience managing product launches
• Proactive critical thinking skills with a solutions-oriented approach

Requirements

• Lead the regulatory review and approval of advertising, promotional, and disease state materials for assigned US products
• Ensure all promotional initiatives comply with FDA regulations and OPDP guidance
• Serve as a key regulatory representative on the Promotional Review Committee (PRC) and Medical Scientific Review Committee (MSRC) for assigned products
• Collaborate cross-functionally to develop product messaging based on clinical data
• Oversee the preparation and timely submission of FDA Form 2253 for assigned US promotional materials
• Provide strategic guidance on conference exhibit activities, speaker programs, and digital communication strategies
• Monitor FDA enforcement actions to perform impact analysis for internal stakeholders
• Support the Director in managing formal communications and regulatory notifications to FDA
• Facilitate the development and implementation of standard operating procedures for the promotional review process and local regulatory affairs responsibilities
• Maintain regulatory documentation and correspondence tracking systems to ensure audit readiness and compliance

Benefits

• Competitive salary range: $150,000 - $170,000
• Short-Term and Long-Term incentive programs
• Comprehensive benefits package including medical, dental, and vision
• Flexible time off (unlimited sick time and flex time)
• 401(k) plan
• Life and disability insurance
• Recognition programs