Reference Number: JO-2102-463612
Rate: £28,000 – 30,000
Job Type: Contract
Location: Cardiff

Clinical Trial Administrator
6-12-month FTC/Contract
Cardiff: Flexible remote working
Up to 30,000 DOE

Cpl Life Sciences are urgently recruiting for an experienced CTA to join one of our Pharmaceutical clients on a fixed term or contract basis. This is a great opportunity to work in a dynamic and progressive business who are currently increasing their portfolio. You will be expected to work independently and therefore 2-3 years experience is required for this role.

Key tasks and responsibilities shall include:
Organise and maintain the paper and electronic TMF
Collation of study documents from monitors
Support Clinical Project Managers with day to day reporting and operational functions
Appropriate filing and organisation of all documentation
Ensure documentation is prepared and collated for regulatory and ethical submissions
Arrange internal and external meetings
Review TMF and SOF for completeness
Assist in setting up study files and folders
Track the distribution of appropriate documentation across sites and vendors
Arrange translation and request signatures for key essential documents
Working independently and proactively

Experience and attributes:
2-3 years experience working as a CTA
Confident IT skills including previously working on the eTMF
Independent and proactive work ethic
Personable with strong communication skills

If this role is of interest to you then please apply or email your CV to sarah.phillips@cpl.com.

Upload your CV and any other relevant file.
I would like to be contacted via SMS
I have read and agree to the Clinical Professionals Group Privacy Policy

Find our privacy policy here