Cpl Life Sciences

Clinical Trials Associate

29 Apr 2021
28 May 2021
Rhianna Bellamy
Full Time
Contract Type
Experience Level
Experienced (non-manager)

Clinical Trials Associate
Location: Surrey (2-3 days WFH)

CPL Life Sciences are currently working with a growing global biopharma company to recruit an experienced Clinical Trials Associate. The company is focused on improving the lives of patients with genetic, metabolic, and life-threatening disorders by developing and commercialising novel treatments. Due to growth and the development of their product pipeline, they require someone to join their team on a permanent basis. The purpose of this role will be to provide overall support to the Clinical Project Manager and Clinical Operations Manager to ensure the successful completion of project deliverables.

Key responsibilities:
Maintaining accurate study files with appropriate QC/QA review
Preparing ethics and regulatory submission documents
Assisting the Clinical team collecting and compiling essential study documents
Supporting the development of study-related documentation, such as monitoring plans
Providing support to ensure monitoring activities are done according to the monitoring plans
Setting up, maintaining, and archiving of study files in the Trial Master File (TMF)

Experience working as a CTA within a pharma, CRO or biotech
The ability to work with cross-functional teams
Strong communication skills
Experience setting up and maintaining TMF

The successful applicant will receive a competitive salary and benefits and will work within a supportive, close-knit team. If you are interested in this role, send your CV to Rhianna.bellamy@cpl.com or apply within

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