Experienced Clinical Trial Administrators needed to start work quickly within a major pharma in Surrey. Must be competent already, good rate of pay.
Superb contract CTA role working with a top 5 pharma company, in beautiful, modern offices in Surrey. Working closely with project managers who are responsible for clinical studies in the UK, this will give you a real insight in to drug development.
Summary of duties:
Preparing, distributing, tracking and filing/archiving of essential study documentation. Preparation and despatch of study supplies and materials (e.g. Site Files) to Investigator Sites.
Direct communication with Country Clinical Study Managers (CCSMs), Clinical Research Site Managers (CRSMs), Therapy Area Team Managers^(TATMs) and Investigator Site staff (if and when deemed appropriate).
In collaboration with CCSM, ensure all documentation, relevant approvals and business systems are in place and up to date to allow timely study medication release to Investigator^Sites.
Qualifications required:
Minimum 2 GCSE (or equivalent) pass in Maths & English or demonstrable competency in written and numeracy skills.
Experience in a previous operational/logistical support role is preferred.
Computer literacy is^essential (word processing, maintaining spreadsheets, compiling presentation slides, with Microsoft Packages). Ability to retrieve information using database searches is also an essential requirement.
Resource planning and management would be an advantage.
Knowledge of ICH-GCP and the UK statutory instrument.
Detailed knowledge and understanding of the CTA role.
Previous experience in a Clinical Research role/setting would be highly advantageous and awareness of ICH-GCP and the UK statutory^instrument would be desirable.