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Clinical Data Manager

Remote
40,000
Permanent
Data & Bioinformatics

Compass Life Sciences are working with a Global Clinical Research Organisation who are recruiting a Clinical Database Manager on a permanent basis. We are considering candidates across the UK and Europe, with fully remote working available and multiple levels of seniority.

More Info

Compass Life Sciences are working with a Global Clinical Research Organisation who are recruiting a Clinical Database Manager on a permanent basis. We are considering candidates across the UK and Europe, with fully remote working available and multiple levels of seniority.

This is an exciting time for our client, as they continue to lead the sector, with their highly innovative suite of technologies that bring their clients ever closer to the clinical data emerging from their clinical trials, with a special focus on Oncology and rare diseases.

As a CRO, our client is made up of highly talented experts from across the sector, focussed on clinical trials, and the data that comes from them. They are a valued partner to many of the top Pharmaceutical and Biotechnology companies in the world, and they have built strong long-standing relationships based on repeated successful delivery of studies, using revolutionary ways of gathering, managing, and analysing data in clinical trials.
Our clients Clinical Data Management Department is at the cutting edge, defining new and more efficient ways to design, capture, manage, review and visualize clinical trial data and they are now looking for a talented Clinical Data Manager to join their team and help drive this change.

In this role, you will be responsible for the delivery of multiple, large or complex projects working with cross functional teams to develop, design, set up and close out of studies. The ideal candidate will have:

  • Considerable experience in clinical data management in an ICH/GCP environment
  • Experience performing the role of a Clinical Data Management functional lead for EDC studies, from clinical database setup to lock
  • A background in all data management start-up activities, including database design, edit check specifications, handling of third-party data and user acceptance testing
  • A strong understanding of data structures e.g. CDISC CDASH and STDM
  • Have experience using reporting and data review tools
  • Is a great communicator and will have experience working in cross functional project teams and with vendors
  • Understand medical terminology, clinical trial methodology and ICH/GCP and other regulations
  • Have managed project budgets, including time spent on data management tasks, and associated timelines and projections

If this sounds like the right move for you in your career and would like more information, please contact Ben Brown on [email protected] or +44(0)2393 874 320 for further information.

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