Clinical Data

Job type:
on-site
Start:
02/2015
Duration:
n.a
From:
Real Staffing
Place:
Cambridge
Date:
03/09/2015
Country:
flag_no United Kingdom
project ID:
864576

Warning
This project is archived and not active any more.
You will find vacant projects in our project database.
The job responsibilities will include:
  • Thorough understanding of Clinical Data Management tasks and assigned protocol(s) with ability to critically evaluate the information in relation to other key project documents and processes.
  • Coordinate, create and maintain the Data Management Plan, creation of CRF Guidelines
  • Ensure assigned actions are completed within the required time frame.
  • Review and approve post production change control study documentation.
  • Maintain all data management study documents in the designated TrialShare area and PMF as required.
  • Contribute to the development and/or revision of Clinical Data Management SOPs and related documentation
  • Gather and consolidate feedback, metrics and status reports from CDM Team Leads to assess CDA performance and quality of deliverables. Escalate any performance and quality issues to PDM.
  • Present CDM function at conferences and external non-study meetings.


If you are interested in hearing about this role, have any questions about this position or would like to register your interest in other positions, please feel free to send your up to date CV or contact me on