Senior Regulatory Affairs Manager - Emerging Markets

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

Job summary

A leading global pharmaceutical company is seeking a Senior Regulatory Affairs Manager to oversee NDA communication and strategies specifically for Emerging Markets. This full-time role, offered on a 12-month contract, involves collaboration with various teams to ensure timely product launches and compliance across multiple regions. As an equal opportunities employer, we encourage applications from all backgrounds.

Responsibilities

• Manage communication and implementation of NDA strategies for Emerging Markets.
• Develop regulatory strategies for product coordination and delivery.
• Serve as Regional Strategy Lead, providing insights and contributing to forums.

Job description

Role: Senior Regulatory Affairs Manager - Emerging Markets

Location:

Remote, UK

Company:

Global Pharmaceutical

Duration:

12-month contract, full-time

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, coordinating with partners, affiliates, supply chain, PV, commercial, and medical teams to optimize NDA filing and launch strategies, ensuring timely delivery in partnership with CRO.
3. Serve as Regional Strategy Lead in RPT for assigned products, 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 a regional office in Central London, operating in over 30 countries with a network of 2500+ contractors. Recognized by FORBES as the 17th best professional staffing firm, we offer expertise across Regulatory Affairs, Pharmacovigilance, QA, QC, Clinical Development, Medical Affairs, and more.

We are an equal opportunities employer and welcome applications from all qualified candidates regardless of race, sex, disability, religion/belief, sexual orientation, or age.