Senior Regulatory Affairs Manager - Emerging Markets

JR United Kingdom; Woking; Remote; GBP 60,000 - 90,000; Full time

Job summary

A leading global pharmaceutical firm seeks a Senior Regulatory Affairs Manager to oversee NDA strategies for Emerging Markets, coordinating with various teams to ensure optimized filing and launch. This full-time remote role spans 12 months and provides a significant opportunity for strategic contribution.

Responsibilities

• Manage communication, development, and implementation of NDA strategies for Emerging Markets.
• Develop regulatory strategies for assigned products, collaborating with internal teams.
• Participate in cross-functional meetings as Regional Strategy lead.

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), working closely with global, regional, and in-country regulatory teams.
2. Develop and deliver regulatory strategies for assigned products, collaborating 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. Participate as a member of the RPT as Regional Strategy lead, providing regional insights and contributing to cross-functional forums, including launch meetings.

About Planet Pharma:

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

Recognized by FORBES as the 17th best professional staffing firm, we have received multiple industry awards. Our expertise spans Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions, Clinical Development, Quality, Biostatistics, and Medical Affairs/Writing.

We are an equal opportunity employer, welcoming applications from all qualified candidates regardless of race, sex, disability, religion, sexual orientation, or age.