Senior Clinical Research Assoicate

England  ‐ Onsite
This project has been archived and is not accepting more applications.
Browse open projects on our job board.

Keywords

Description

Main responsibilities (to include but not limited to):

* Investigator identification and selection.
* Co-ordination of ethics committee and regulatory authority applications and approvals.
* Pre trial procedures including collation of necessary documentation.
* Organisation, attendance and/or presentations at investigator meetings.
* Initiation, monitoring and close-out of investigational sites
* Training of site staff to trial specific and industry standards.
* Supervision and/or distribution of trial supplies, including the trial drug (investigational medicinal product).
* Protocol and Case Report Form (CRF) development.
* Archiving of trial documentation and correspondence.
* Clinical Trial Report and manuscript for publication (occasional).

To find out more about Real please visit www.realstaffing.com
Start date
03/2014
From
Real Staffing
Published at
02.04.2014
Project ID:
687939
Contract type
Permanent
To apply to this project you must log in.
Register