Senior CRA

Reference:

Job Type: Permanent
Location: United Kingdom, Yorkshire,
Salary: Competitive

Start Date: Marh 2012

Key Tasks

Provide full support to all aspects of clinical research programmes to ensure that studies are planned, monitored and reported in accordance with all SOP requirements within agreed timescales with defined clinical research strategy.
Maintain the highest ethical, clinical and scientific standards ensuring both the safety and well being of trial participants and good/rigorous scientific practice.
Keep abreast of international legislation and other requirements concerning clinical research. Prepare and submit submissions for the approval of clinical investigations to regulatory and ethics committees.
Keep abreast of developments in clinical research and the clinical literature in therapeutic areas of responsibility.
Ensure that the preparation of clinical trial protocols, case report forms and consent documentation is in accordance with all ethical and regulatory requirements.
Monitor the clinical research programme in accordance with Good Clinical Practice and ISO 14155 requirements and provide regular feedback to clients on the progress of trials..
Maintain compliance with SOP's and participate in SOP development and improvement.
Maintain a high standard of housekeeping and filing accuracy.

Applications are handled online where you will be able to upload your CV.