Description
One of Volts leading Pharmaceutical clients are looking to recruit as CTA into their Surrey office for a 12 month contract.
Summary of Role
The role involves a significant level of coordination of document management oversight with the Country Clinical Study Manager
*Generating essential documents from templates (eg, one page CVs, financial disclosure forms, FDA 1572) and other study-specific documents/tools for study sites (eg, informed consent forms)
*Preparing, Quality Checking, distributing, tracking and filing of essential documents within our electronic Trial Master File
*Preparation, dispatching and tracking of study supplies and materials (eg Site Files) to Investigator Sites.
*In collaboration with 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 dispatch 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.
Please forward your CV immediately for consideration into this role as it is an urgent fill.