Massachusetts Licensed Regulatory Affairs Lead

A company is looking for an Associate Director, Global Regulatory Affairs-Advertising and Promotion Review Lead.

Key Responsibilities

Serve as the subject matter expert for assigned products and projects in the advertising and promotion review process

Act as a regulatory advisor in the core Medical, Legal, Regulatory review functions for commercial and medical material

Lead global Commercial Material Review Process meetings and manage team dynamics to ensure alignment on promotional strategies

Required Qualifications

Bachelor's Degree in a science-related field is required; Master's Degree preferred

A minimum of 3 years' experience in material review and approval processes for pharmaceutical / biologics promotion

Understanding of ABPI, EFPIA, and other international codes and guidance related to advertising and promotion

Experience in the development and review process of prescription medicine promotion

Previous experience in an advertising and promotion role is preferred