Clinical Trials Administrator

Job type:
on-site
Start:
January 2012
Duration:
12 months
From:
Computer 2000
Place:
Surrey
Date:
01/06/2012
Country:
flag_no USA
project ID:
292462

Warning
This project is archived and not active any more.
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Our client is looking for a Clinical Trials Administrator for a 12 month assignment based in Surrey.

You will be expected to have:

  • Experience with other key study documents (helping generate protocols amendments EC submissions)
  • Knowledge of SUSAR/safety reporting
  • Knowledge of invoice/payment tracking
  • Ability to lead meetings (ad hoc) and effectively take minutes/actions
  • In collaboration with the Study Manager, ensure all documentation, relevant approvals and business systems are in place and up to date to allow timely study medication release to Investigator Sites.
  • Ensure timely internal reporting and despatch of periodic (monthly and annual) safety reports to relevant ethics committees.
  • Provide general and ad hoc support to Study Teams from study start up to close out using specified business systems
  • Liaise with Business Support Managers to maintain system knowledge as current and valid within the Subject Matter Expert role.
  • Train new starters in business systems and provide ongoing support for key customers of these systems.

In accordance with our commitment to equality, we welcome applications from candidates of any age, disability, ethnicity, gender or religion for this role.