Senior Regulatory Affairs Manager - Emerging Markets

JR United Kingdom; Uxbridge; Remote; GBP 60,000 - 85,000; Full time

Job summary

A leading global pharmaceutical company is seeking a Senior Regulatory Affairs Manager to oversee NDA strategies in Emerging Markets. The role involves collaborating with various teams to optimize product launch strategies. This remote position requires expertise in regulatory affairs and strategic management within the pharmaceutical industry.

Responsibilities

• Manage communication and implementation of NDA strategies in Emerging Markets.
• Develop regulatory strategies and coordinate with global teams.
• Participate as Regional Strategy lead in cross-functional forums.

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 with global, regional, and local regulatory teams.
2. Develop and deliver regulatory strategies for assigned products in these regions. Coordinate with partners, affiliates, supply chain, PV, commercial, and medical teams to optimize NDA filing and launch strategies. Ensure strategy delivery aligns with agreed timelines, working with CROs.
3. Participate as a Regional Strategy lead in the RPT for assigned products, providing regional insights and contributing to cross-functional forums, including launch meetings.

About Planet Pharma:

Planet Pharma is an American-based employment agency providing global staffing services, headquartered in Chicago with a regional office in Central London. We operate in over 30 countries with a network of 2,500+ contractors and offer permanent and direct hire recruitment services.

Recognized by FORBES as the 17th best professional staffing firm, we pride ourselves on industry expertise and strong client relationships. Our services span Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions, Clinical Development, Quality, Biostatistics, and Medical Affairs.

We are committed to diversity and equal opportunities, welcoming applications from all qualified candidates regardless of race, sex, disability, religion, sexual orientation, or age.