Data Manager

UCL
Charing Cross, United Kingdom
yesterday

Role details

Contract type
Temporary contract
Employment type
Full-time (> 32 hours)
Working hours
Regular working hours
Languages
English

Job location

Charing Cross, United Kingdom

Tech stack

Microsoft Access
Microsoft Word
Microsoft Excel
Text Processing
Data Management

Job description

About us

The Comprehensive Clinical Trials Unit is a specialist unit set up within the Institute of Clinical Trials and Methodology with a specific remit to design, conduct, analyse and publish clinical trials and other well-designed studies.

About the role

We currently have a vacancy for full-time Data Manager to work within the Unit. The post holder will report to the Trial Manager. A job description and person specification is available at the bottom of the page. Please provide your CV and a cover letter explaining how your skills and experience are applicable to the role.

About you

An enthusiastic individual is sought for this post which is based in Holborn, London. The primary role of the post holder is to assist with the efficient collection, processing, validation, and quality assurance of data from trials.

The successful applicant will have experience of data entry and data management, excellent communication skills and experience of working on a clinical trial or in a medical research environment. Experience of word processing, using Microsoft Word, Excel and Access are also essential requirements for this post.

The role holder will be responsible to the Trial Manager and the post is funded until 31^st January 2028.

Interviews will be held in person on Tuesday 2nd June.

Please note that we are unable to provide sponsored visa for this role.

A job description and person specification can be accessed at the bottom of this page. If you have any queries regarding the vacancy please contact CCTU Enquiries at cctu.eat-up@ucl.ac.uk

Customer advert reference: B02-10509

Requirements

An enthusiastic individual is sought for this post which is based in Holborn, London. The primary role of the post holder is to assist with the efficient collection, processing, validation, and quality assurance of data from trials.

The successful applicant will have experience of data entry and data management, excellent communication skills and experience of working on a clinical trial or in a medical research environment. Experience of word processing, using Microsoft Word, Excel and Access are also essential requirements for this post.

The role holder will be responsible to the Trial Manager and the post is funded until 31^st January 2028.

About the company

The Comprehensive Clinical Trials Unit is a specialist unit set up within the Institute of Clinical Trials and Methodology with a specific remit to design, conduct, analyse and publish clinical trials and other well-designed studies.

Apply for this position