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 [email protected]