Senior Associate / Associate Manager – Regulatory Affairs (UK)
Contract | Fully Remote | Inside IR35
MSI Pharma is partnering with a pharmaceutical organisation to appoint a Senior Associate / Associate Manager, Regulatory Affairs to support UK regulatory activities. This opportunity is well suited to experienced UK Regulatory Affairs professionals with hands‑on MHRA exposure.
Contract details:
- Initial 12‑month contract
- Hourly freelance rate
- Inside IR35
- Engagement via PAYE through MSI Pharma
- Fully remote (UK‑based)
The Role
You will support UK marketing authorisation and lifecycle management activities, contributing to regulatory strategy and execution across development and marketed products. The role involves close collaboration with cross‑functional teams and interaction with UK regulatory authorities.
Key Responsibilities
- Coordinate preparation, submission and maintenance of UK regulatory submissions, including MAAs, variations and lifecycle activities
- Support regulatory strategy development aligned to business and development objectives
- Manage regulatory agency queries, commitments and responses in collaboration with internal subject matter experts
- Support agency meetings and preparation of briefing documentation
- Provide regulatory input at study and project level within cross‑functional teams
- Maintain up‑to‑date knowledge of UK regulatory requirements and communicate regulatory intelligence as needed
Required Experience
- Degree in a scientific or life sciences discipline (or equivalent experience)
- 5+ years’ experience in Regulatory Affairs within the pharmaceutical industry
- Demonstrated experience working with the MHRA and UK regulatory procedures
- Hands‑on experience with UK MAAs, labelling and lifecycle management
- Strong communication skills and ability to operate effectively in cross‑functional environments
If you are an experienced UK Regulatory Affairs professional seeking a fully remote contract role, I would welcome the opportunity to discuss this further.
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