Sr. Clinical Data Manager (CP04HM734)
Horsham, England, United Kingdom
5d ago

Why Cmed?

Cmed occupies a unique position in the clinical research industry, not only as an expert in the operational delivery of clinical trials for immuno-oncology and cell & gene therapies, but also as a developer of its own technologies for managing clinical data.

This is a very exciting time to join Cmed, as we continue to leverage our considerable expertise in the delivery of clinical trials with our game-changing EDC and eSource platform, encapsia™.

Our unique combination of operational expertise and the latest technology helps reduce the costs and increase the speed of developing new medicines, essential to both improving and saving the lives of patients.

Cmed’s 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 we are now looking for a talented Senior Clinical Data Manager to join our team and help drive this change.

The Role :

You will provide leadership for clinical data management tasks and be responsible for the delivery of multiple, large or complex projects.

Depending on your experience, there may also be opportunities to specialize in certain data management aspects and mentor junior team members.

This role can be remote anywhere in the UK or EU, or office based in West Sussex.

This role could be perfect for you if you :

  • Have led large or complex EDC studies and study teams
  • Have experience with defining data strategies and data flows for complex trials involving multiple data sources (incl.
  • central lab, eCOA / ePRO, IRT)

  • Have hands-on experience in all end-to-end data management activities, including database design / UAT, third-party vendor management, (central) data review and close-out
  • Understand data structures e.g. CDISC CDASH and STDM
  • Have experience using reporting and data review tools
  • Are a great communicator and have experience working with cross functional teams and direct client interactions
  • Understand medical terminology, clinical trial methodology and ICH / GCP and other regulations
  • Have proactively managed project budgets, including time spent on data management tasks, and associated timelines and projections
  • Are great at planning, well organized and can work calmly under pressure
  • Have significant data management experience and a degree level qualification or equivalent experience
  • Having been exposed to Central / Risk-based Monitoring and Real-World Data is a plus
  • What we offer :

  • A dynamic, friendly and supportive team
  • Innovative and exciting technologies
  • Mentorship and training to further develop your skills
  • Home or office-based location
  • Competitive compensation package
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