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Clinical Study Associate - Biotech - UK

Employer
RBW Consulting
Location
Aylesbury, Buckinghamshire (GB)
Salary
£30,000 - £38,000
Start date
27 Feb 2019
Closing date
29 Mar 2019

Job Details

Working within pain management therapies, this role will have involvement in a yet-to-be initiated clinical study set to run across 4 or 5 European companies. You will be integral in supporting the Clinical Team as the study gets underway over the coming year.

 

 

 

Responsibilities:

 

  • Prepare, archive and maintain essential documentation according to SOPs; Management and maintenance of the Trial Master File according to appropriate regulations;  Provide logistic support for study supplies to sites; Prepare relevant documents for Study Drug Approval and release; Collaborate with preparation of required documents for submission to IRBs/ IECs and CA.

 

 

Requirements:

 

  • Relevant Life Sciences degree; +3 years' experience working as a Clinical Trial Administrator; Extensive experience in TMF management including set-up and/or maintenance is essential; Good knowledge of requirements regarding essential documentation and GDP; Knowledge of ICH-GCP guidelines and clinical research regulatory environment.

 

 

This is one of several positions I am currently recruiting for so do please get in touch for a confidential discussion around your current situation and what your ideal next move would be.

 

 

 

To make an application please feel free to apply via this website, I am also available on LinkedIn to message regarding the role and will accept all invitations that refer to this advert - look for Dominic Mitchell at RBW Consulting.

 

 

 

Please note that owing to the high volume of applications we receive for our roles, if you have not received a response within 48 working hours, do please consider your application unsuccessful.

 

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