Regulatory Affairs Project Manager

3 weeks ago


High Wycombe, Buckinghamshire, United Kingdom Harris Lord Life Sciences Full time
Regulatory and Clinical Project Manager

Location: High Wycombe - Hybrid (up to two days a week working from home)

Are you looking for a challenging role in Regulatory Affairs within the Medical Device industry? This UK-based company is seeking a skilled Regulatory and Clinical Project Manager to join their team in High Wycombe. The ideal candidate will have a strong background in Regulatory Affairs and Clinical experience, with a project management qualification (e.g., PRINCE2 or other Project Management training/qualification).

As a Regulatory and Clinical Project Manager, you will be responsible for supporting British manufacturing by working for this UK Medical Device company. You will spend most of your time in the beautiful offices in High Wycombe, with the ability to work hybrid up to two days per week. The company offers a great array of benefits with team wellness at its heart.

Key responsibilities include:

  • Leading projects from initiation to closure, ensuring timely delivery and high-quality results.
  • Collaborating with cross-functional teams to develop and implement regulatory strategies.
  • Providing expert advice on regulatory matters, ensuring compliance with relevant laws and regulations.
  • Developing and maintaining relationships with key stakeholders, including customers, suppliers, and regulatory bodies.


This is an excellent opportunity for a motivated and experienced Regulatory and Clinical Project Manager to join a dynamic team and contribute to the success of the company. If you are passionate about Regulatory Affairs and have a strong background in project management, we encourage you to apply.

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