Senior Regulatory Affairs Manager - Emerging Markets

JR United Kingdom; Brighton; Remote; GBP 70,000 - 100,000; Full time

Job summary

A leading global staffing firm seeks a Senior Regulatory Affairs Manager specializing in Emerging Markets. The role involves managing regulatory strategies and product launch collaborations across MEA, Turkey, CIS & Russia, and Central Eastern Europe. As part of a diverse team, you will ensure compliance and drive timely product approvals.

Responsibilities

• Manage communication and implementation of NDA and line extension strategies in Emerging Markets.
• Develop regulatory strategies for product launches, collaborating with teams and partners.
• Serve as Regional Strategy lead within the Regulatory Process Team.

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), working closely with global, regional, and in-country regulatory teams.
2. Develop and deliver regulatory strategies for assigned products, collaborating with partners and 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 Regional Strategy lead for assigned products within the Regulatory Process Team (RPT), providing regional insights and participating in cross-functional forums, including launch meetings.

About Planet Pharma:

Planet Pharma is a global staffing services provider with headquarters in Chicago and an EMEA regional office in Central London. Recognized by FORBES as the 17th best professional staffing firm, we operate in over 30 countries with a network of more than 2,500 active contractors. We specialize in Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions, Clinical Development, Quality, Biostatistics, and Medical Affairs/Writing.

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