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Clinical Trial Specialist

Buckinghamshire   •  Negotiable  •  Permanent, Full time


Clinical Trial Specialist

Location: Buckinghamshire (hybrid working)

A multinational healthcare company are looking for a Clinical Trial Specialist to join their consumer health division. This role offers excellent opportunities to progress as the team is currently being built as a new entity for their consumer health division. Currently they have roles within dermatology and self-care.

The purpose of this role will be to support the operation aspects of the clinical research activities.

Key responsibilities:

  • Writing study protocols and amendments
  • Training staff on study-specific protocol procedures
  • Preparing study-specific documents including informed consent forms (ICFs)
  • Serving as the primary point of contact for selected external service providers (ESPs)
  • Ensuring sponsor oversight by monitoring the progress of studies and performance of ESPs
  • Setting-up and maintaining Trial Master Files
  • Managing study timelines including key milestones
  • Tracking and approving invoices
  • Overseeing Monitors and carrying out monitoring as required

Requirements:

  • A degree in a relevant disciple
  • Experience within clinical trials, ideally consumer health
  • Vendor management experience
  • Study document knowledge including TMF

If you would like to hear more, please apply within or send your CV to Rhianna.bellamy@cpl.com

  • Agency: Cpl Life Sciences
  • Contact: Rhianna Bellamy
  • Reference: JO-2201-483632
  • Updated: 17th January 2022
  • Expires: 14th February 2022

Cpl Life Sciences

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