job details for:
Medical Devices – Clinical Trial Project Manager – West Sussex

Medical Devices – Clinical Trial Project Manager – West Sussex (Job Ref: WR/JOBS/25239-11660)

Job Description :

Job Summary

Medical Devices – Clinical Trial Project Manager – West Sussex

UK. 

Excellent Package

Our client is part of one of the largest global technology companies, and as a leading medical device company, they are pioneers within respiratory medicine.  As part of ongoing business expansion, we are recruiting a Clinical Trial Project Manager to oversee and co-ordinate a team (already in established) to conduct a regulatory standard prospective clinical trial that would lead to submission.  This excellent opportunity will be for 3 days per week and will cover 9 months initially with the possibility of extension.

The Role

The Clinical Trial Project Manager will complete the development of the clinical trial protocol and to ensure that protocol will meet the regulatory requirements necessary to secure successful approval by the MHRA and EU regulatory authorities.  You will establish then maintain an up to date Project Plan to ensure that the study timelines are adhered to and that Project milestones are met.  Ensure that all CRO’s selected, contracted and used are fit for purpose and are selected and contracted in accordance with the appropriate SOPs.  The Clinical Trial Project Manager will ensure that all clinical trial supplies, medical devices and supporting patient documentation required are written, printed or manufactured in a timely manner and are written, printed  or manufactured  to the relevant regulatory standards.  You will Ensure that the monitoring of the sites by the CRO is efficient, thorough and in line with the requirements of the protocol and GCP.

The Person

With a background in medicine, science or other relevant discipline, you will have a proven track record within clinical research in a similar role.  You must have extensive clinical project management and line management experience to ensure that you can ‘hit the ground running’. You will be an exceptional communicator and decision maker with a thorough knowledge of ICH GCP and relevant regulations for the conduct of clinical trials.

  
Key Words

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