Global Regulatory Affairs Lead - Patient Access Programs

Date posted: 2026-05-21T00:00:00

Location: Greater London, London, UK, WC2N 5DN

Company: WEP Clinical Ltd

Role: Regulatory Affairs Manager to oversee regulatory submissions and strategy for clinical trials. This role requires 5 years of regulatory experience and expertise in EU and FDA regulations. Responsibilities include managing licenses and partnering across departments for seamless project execution.

Responsibilities

Oversee regulatory submissions and strategy for clinical trials.

Ensure compliance with EU and FDA regulations.

Manage licenses and partner across departments for seamless project execution.

Requirements

5 years of regulatory experience

Expertise in EU and FDA regulations

Benefits

Private healthcare

Long-term illness cover

Annual leave

Join a mission-driven organization that prioritizes innovation and patient outcomes.

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WEP Clinical Ltd in Greater London seeks a Regulatory Affairs Manager to oversee regulatory submissions and strategy for clinical trials. This role requires 5 years of regulatory experience and expertise in EU and FDA regulations. Responsibilities include managing licenses and partnering across departments for seamless project execution.The position offers a range of benefits including private healthcare, long-term illness cover, and annual leave. Join a mission-driven organization that prioritizes innovation and patient outcomes.
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