Manager Clinical Regulatory Affairs

This Manager Clinical Regulatory Affairs role is focused on preparing and submit new Marketing Authorisation Applications (MAAs) supporting international countries within the Emerging markets region. It would suit someone who can bring careful technical judgement and practical problem-solving to the role.

Known job details

• Contract: Permanent
• Work model: Hybrid
• Additional detail: Hybrid working.

Likely focus of the role

• Preparing and submit new Marketing Authorisation Applications (MAAs) supporting international countries within the Emerging markets region.
• Supporting global expansion through the submission of registration dossiers for existing products.
• Leading dossier remediation activities, including aligning legacy registrations with current regulatory requirements to enable geographic expansion.

Requirements mentioned

• Degree‑qualified in a Life Sciences discipline or related field.
• Minimum 5 years’ experience supporting international regulatory markets.
• Proven experience managing new MAAs, global expansion of existing products, and extensive lifecycle maintenance (essential).