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Imperial College London

Country: United Kingdom

Specific Location: London

Job Title: eCRF Designer / Developer

Type of Job: Permanent

Job Description:

Job summary
Imperial Clinical Trials Unit (ICTU) has a vacancy for a Clinical Trials eCRF Designer / Developer within the Clinical Data Systems (CDS) team reporting to the Development Team Leader. The CDS team develops and supports electronic data capture (EDC) system for clinical trials and comprises three teams with expertise in different areas so collaborative working across the team is essential.

Duties and responsibilities
You will be responsible for delivering high quality eCRFs for healthcare related trials through the lifecycle of design, development and unit testing. You will also be responsible for ensuring that the solutions delivered are both fit for purpose and compliant with regulatory requirements and delivered within strict timelines.

The Clinical Trials eCRF Designer / Developer will be expected to use OpenClinica to author, design and develop eCRF and Edit Checks for EDC systems based on user requirement specifications, following standards and methodologies. You are expected to be involved in trials at various stages of the development lifecycle.

Essential requirements
You should hold a degree or equivalent in computer science or a relevant subject and/or relevant experience. Previous experience with EDC (Electronic Data Capture) systems is essential e.g. InForm™. A background in clinical data management of eCRF design/development is also required.

You should understand the key stages and processes involved in the implementation of eCRFs, together with use of formal development life cycle methodologies. To add to this, you should have good knowledge of GCP and other regulatory requirements for computerised systems supporting clinical trials in the UK and International markets. You should also understand ICH-GCP and other applicable regulations associated with clinical trial data handling.

Experience of working to, authoring and reviewing Standard Operating Procedures, Working Instructions and User Guides is essential as well as awareness of General Data Protection Regulations (GDPR) and how it relates and applies to Clinical Trials.

Further information
The post is full-time and open ended, and is based at the Imperial Clinical Trials Unit, Stadium House, White City Campus (currently working remotely).

For an informal discussion about the post please email Abinithya Udayakumaran,

Closing Date: April 18, 2021

Website/URL for further details: click here

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