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Senior Regulatory Affairs Manager - Emerging Markets

JR United Kingdom

Stockport

Remote

GBP 60,000 - 85,000

Full time

2 days ago
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Job summary

A leading global pharmaceutical company seeks a Senior Regulatory Affairs Manager for Emerging Markets to lead regulatory strategy and implementation. Responsible for managing NDA strategies, working with cross-functional teams, and ensuring timely product launches, this remote position requires strong collaboration skills and regional expertise.

Responsibilities

  • Manage communication and implementation of NDA strategies for Emerging Markets.
  • Develop regulatory strategies for assigned products in specified regions.
  • Serve as a Regional Strategy lead within the RPT for assigned products.

Job description

Role: Senior Regulatory Affairs Manager - Emerging Markets

Location:

Remote, UK

Company:

Global Pharmaceutical

Responsibilities:
  1. Manage communication, development, and implementation of NDA and major line extension strategies for assigned products in Emerging Markets including Middle East Africa (MEA), Turkey, CIS & Russia (TCR), and Central Eastern European Markets (CEE). Collaborate closely with global, regional, and in-country regulatory teams.
  2. Develop and deliver regulatory strategies for assigned products in the specified regions, working with partners, affiliates, supply chain, PV, commercial, and medical teams to determine optimal NDA filing and launch strategies, ensuring timely delivery in partnership with CRO.
  3. Serve as a Regional Strategy lead within the RPT for assigned products, providing regional insights and participating in cross-functional forums, including launch meetings.
About Planet Pharma:

Planet Pharma is an American-headquartered employment business providing global staffing services, with a regional office in Central London. We operate in over 30 countries, supporting a network of over 2500 active contractors worldwide. Recognized by Forbes as the 17th best professional staffing firm, we specialize in Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions, Clinical Development, and Medical Affairs, among others.

We are committed to equal opportunity employment and welcome applications from all qualified candidates regardless of race, sex, disability, religion, sexual orientation, or age.

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