Summary of Position:
Position Responsibilities:
- Holds primary responsibility for development of product labeling, including core labels and local US and EU labeling,
- Conduct research related to labeling precedent, regional regulatory policies, and other topics, as necessary, to advise on potential labeling impact, strategy, or outcome.
- Lead the Label Working Group (LWG) for assigned programs/products to drive alignment of labeling content and strategy and represent the regulatory labeling function at governance meetings.
- Provide input into strategy for Health Authority interactions regarding all aspects of labeling, including submissions, responses to questions, and negotiations.
- Accountable for compliance with health authority requirements, labeling governance requirements and associated business processes.
- Leads the continuous improvement of labeling processes to enhance efficiency. Provides department/company training on labeling practices and policies.
- Provide assistance to the Regulatory Affairs Advertising and Promotion function to support the commercialization of marketed products.
Candidate Requirements:
- Bachelor’s degree or advanced scientific degree (MSc, PhD, PharmD) preferred
- 5+ years of direct experience in regulatory affairs global labeling
- Experience that demonstrates ability to create development labeling processes and documents (initial CCDS).
- Ability to research and understand complex scientific and regulatory information and distil important aspects for impact to labeling.
- Strong project management skills to plan, prioritize, lead, and execute individual work, and teamwork related to regulatory labeling in a systematic and efficient manner.
- In-depth and practical knowledge of labeling requirements globally (USPI and SmPC required), including development and life-cycle management of local PIs and PILs.