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Senior Regulatory Affairs Manager - Emerging Markets

JR United Kingdom

Worcester

Remote

GBP 70,000 - 90,000

Full time

2 days ago
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Job summary

A leading global pharmaceutical company is seeking a Senior Regulatory Affairs Manager to oversee NDA strategies for Emerging Markets. This remote role requires collaboration with various teams to develop and implement regulatory strategies, ensuring delivery within timelines. The position is full-time for a duration of 12 months, offering a competitive salary in line with industry standards.

Responsibilities

  • Manage communication, development, and implementation of NDA and major line extension strategies.
  • Develop and deliver regulatory strategies for assigned products.
  • Serve as Regional Strategy Lead for assigned products within the RPT.

Job description

Role: Senior Regulatory Affairs Manager - Emerging Markets

Location:

Remote, UK

Company:

Global Pharmaceutical

Contract Duration:

12 months, full-time

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

Planet Pharma is a global staffing services provider headquartered in Chicago with an EMEA regional office in London. Recognized by FORBES as the 17th best professional staffing firm, we operate in over 30 countries with a network of 2,500+ active contractors. We specialize in Regulatory Affairs, Pharmacovigilance, QA, QC, Clinical Development, and related fields. We are committed to equal opportunity employment and welcome applications from all qualified candidates.

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