OpenClinica V4.0

OpenClinica V4.0 is a fully GCP compliant, all in one platform, cloud-hosted system where the eCRFs are designed in-house by the ICTU Clinical Data Systems Team.

OpenClinica allows for a seamless and integrated user experience through the following modules - Enterprise (EDC), Participate (ePRO and eCOA), Randomize (IVRS and Supply), Insight (Reporting) hosted on the OpenClinica Cloud.

If requesting the use of OpenClinica, please contact cds_services@imperial.ac.uk

A recent article relating to OpenClinica, with input from CDS Team Leaders as well as the RIO, ePARCA-R and CURESPONSE study teams, can be found here.

Our Service benefits in OpenClinica V4.0

CDS Services
  • Easy and fast electronic capture through ultra-capable, user-friendly eCRFs
  • Real-time edit checks, skip logic and auto save of data input
  • Full in-built audit trail of data entry and changes
  • On-line data entry, monitoring and data sign-off which supports Clinical Data Management activities
  • Randomisation and Drug Supply Management, track drug kits and monitor inventory
  • Patient reported outcome (ePRO and eCOA)
  • Reporting of operational and clinical data in real time
  • Data extracts of the data for analyses
  • Disaster recovery provision
  • Supports compliance with legislation and regulatory guidance on clinical research management
CDS Services
  • Design, develop and build study specific eCRFs
  • System/ User acceptance testing of the study specific eCRFs
  • Release management of production version for web-based access at all study centres / sites for all study users
  • Role based training and access for site and sponsor users
  • User support for the duration of the study
  • Database maintenance, secure UK cloud hosted data storage and backup facilities
  • Database Lock and archive extract
  • Read only access to data after database lock

Short-term Clinical Trial Manager vacancy

We are looking for an experienced Clinical Trial Manager to join our supportive team on a short-term basis to help with the day-to-day management of a phase 2 clinical trial.

This is a full-time, short-term contract for up to 6 months and is available immediately.

For more information, please see the Short term Trial Manager advert and Short-term Clinical Trial Manager JD and Person Spec.

Should you wish to apply, please do so by EOB on Monday 23 February. Be sure to include a detailed supporting statement with your CV as we will not consider your application without this. 

 

The Collaborations Section is currently being updated. 

If your request falls under one of the Therapeutic areas details for the relevant email can be found on the Therapeutic Area Contact Details Page.

For commercial sponsors

Visit our dedicated website for commercial sponsors interested in working with ICTU.