DOCS Global

Clinical Trial Associate office-based In Cambridge

Cambridge, UK
05 May 2021
21 May 2021
Full Time
Contract Type
Experience Level
Experienced (non-manager)
As a CTA you will assist Managers in fulfilling its site management activities and obligations in relation to clinical studies as the primary sponsor of those studies.

You will provide vital support to all study related activities: study start-up activities, including creating site folders, collating, preparing and maintaining documents, updating systems, supporting close out activities

You will ensure collection, review, track and provision of appropriate clinical documents to support regulatory submission and to perform IRB/IEC submissions including when appropriate preparation and submission of all documents to the central and/or local committee

You will organise and participate in Investigator meetings and monitor workshops as required within budget guidelines

You will provide administrative support such as word processing, photocopying, faxing, filing, managing correspondence, presentations preparation, basic computer software support

What is required:
* BA/BS/BSc in the life sciences or RN
* Clinical trial administration and coordination experience
*Work experience in life sciences or medically related field, including biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
* Work involving data entry into systems/databases and/or business support role

What is offered

• Full-time career opportunity
• Scope for career progression
• Excellent structured training for all new starters
• Salary will be offered depending on level of experience and skills
• Permanent contract of employment with company perks and benefits
• Company benefits to include 23 days annual leave plus UK bank holidays, pension, medical health insurance, etc.
• Office-based in Cambridge (UK) - some homeworking flexibility could be offered after the training period

For full job details and to apply, please email e today at


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