Senior Regulatory Affairs Lead – UK & MHRA Strategy

Apsida Life Science

Greater London

On-site

GBP 60,000 - 80,000

Full time

14 days+

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Job summary

Apsida Life Science is seeking a Senior Regulatory Affairs Manager to support their UK portfolio. The role involves managing a small team and acting as the primary Regulatory contact for an identified therapeutic area.

The ideal candidate will have significant experience with UK regulatory processes, proven line management experience, and a degree in Life Sciences or a related field. Responsibilities include developing regulatory strategies and ensuring compliance with UK legislation.

Qualifications

  • Significant experience within UK regulatory processes and MHRA interactions.
  • Must have proven, recent line management experience.
  • Experience managing regulatory submissions and lifecycle activities.

Responsibilities

  • Acts as the primary Regulatory contact for identified therapeutic area.
  • Develop regulatory strategies and timely submissions to the MHRA.
  • Ensure compliance with UK legislation for medicines, clinical trials and PIPs.

Skills

UK regulatory processes
MHRA interactions
Line management experience
People skills

Education

Degree in Life Sciences or a related field

Job description

Apsida Life Science is seeking a Senior Regulatory Affairs Manager to support their UK portfolio. The role involves managing a small team and acting as the primary Regulatory contact for an identified therapeutic area.

The ideal candidate will have significant experience with UK regulatory processes, proven line management experience, and a degree in Life Sciences or a related field. Responsibilities include developing regulatory strategies and ensuring compliance with UK legislation.

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