Director, Regulatory Affairs Advertising/Promotion

The Director will partner with all Regulatory Affairs functions, Medical Affairs, Legal, Compliance, Commercial and International distributors and will serve as a key member of the Medical/Legal/Regulatory (MLR) Review Committee. • Serve as an expert resource for regulatory advertising/promotion advice across departments. • A minimum of 10 years of biopharmaceutical industry experience, with a minimum of 8 years of experience in the regulatory review of advertising/promotional materials for prescription drug and/or biologic products. • Extensive in-depth knowledge of regulatory requirements associated with advertising and promotion of prescription drug products, and experience in applying such requirements is required. The ability to be productive and successful in such a work environment is critical.