Description
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.