The Senior Director, Regulatory Affairs Advertising, Promotion (Ad/Promo), and Labeling is a critical leadership role responsible for developing and executing regulatory strategy for all product communications and core labeling. This leader will ensure that all commercial and non-promotional materials, as well as core and local product labeling, are compliant with US FDA, EMA, and other relevant global regulations. The role requires expert-level interpretation of complex regulatory requirements and a proven ability to lead and influence cross-functional teams to achieve both compliance and business goals.
Advertising & Promotion Strategy and Oversight
Labeling Strategy and Management
Leadership and Compliance Management
Supervision Exercised:
Team of 1-4
BS or MS with requisite experience and demonstrated capability. Advanced degree (MD, Ph D, PharmD) preferred
10+ years required of regulatory pharmaceutical industry experience and extensive experience (at least 7 years) in advertising and promotion regulatory affairs including participation on PMRCs, or equivalent experience
Thorough understanding of regulatory requirements for compliant advertising and promotional materials
History of providing creative solutions to Commercial and Medical Affairs teams exhibiting superior judgment and a balanced, realistic understanding of issues
Outstanding interpersonal and communication (written and verbal) skills
Attention to detail and highly organized
Fluency in English as business language
Ability to travel up to 20% of the time domestically and internationally
Experience working with Veeva PromoMats
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