Regulatory Project Manager

CK Group are recruiting for a Regulatory Project Manager to join a biopharmaceutical company who are based in both Uxbridge and Cambridge on a contract basis until the end of 2024.
Company:
Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology.
Location:
The role is predominately home based, but you will need to be able to get to their offices in Uxbridge and Cambridge for team meetings approximately once a month
Salary:
£30.16 per hour PAYE or £39.77 per hour UMB
Regulatory Project Manager role:

• Manage complex projects focusing on in vitro diagnostics regulations
• Resource allocation
• Full life cycle management to ensure all project activities/requirements are met
• Internal and external Stakeholder management

Your Background:

• Previous experience in Regulatory Project Management in the pharmaceutical, medical device, clinical trials or healthcare industries
• A good knowledge of medical device regulations or IVDR.
• Experience with SharePoint and detail orientated

Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 56410 in all correspondence.