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Lead Clinical Data Manager

Zoek Pin - City of London - This Area Only

Competitive

Permanent (Full time)

At DOCS Global, an ICON Clinical Company, as part of large technical clinical data operations FSP with a TOP 10 Pharma company, we are currently recruiting for a number of experienced Lead Clinical Data Managers to join us across a number of European countries (UK, Ireland, Germany, Spain, Belgium, Netherlands, Poland & South Africa).

Please make an application promptly if you are a good match for this role due to high levels of interest.

Title: Lead Clinical Data Managers Duration: Full Time Permanent Employment Location: Multiple EU countries; UK, Ireland, Spain, Germany, Belgium, Netherlands, South Africa and Poland

  • Home Based in these countries.

Responsibilities:

  • Provide data management support, oversight and accountability for one or more clinical trials.

  • Take a leadership role with the CRO/Vendors, trial customers and other internal & external partners to align & confirm data management expectations for assigned trials

  • Review clinical data management documents

  • Plan & track content, format, quality, and timing of clinical data management deliverables, including, but not limited to, CRF, data review plan, QC plan, oversight plan, database release plan, final datasets, submission plan and archival

  • Ensure inspection readiness of all Data Management deliverables; Participate in regulatory and internal/sponsor audits

  • Present and train at investigator and monitor meetings as needed.

  • Perform trial level oversight as per in oversight plan, QC process and work instructions with minimal direction from Data Management Leaders Education / Experience Requirements:

  • Bachelor’s degree or equivalent, in Health or Science discipline with experience in clinical research.

  • 5 years of Clinical Data Management experience; with prior experience in Data Management Project Management / Oversight management and experience in Vendor Management as well.

What we offer:

  • 100% home based (in the above countries)

  • Full-time permanent roles

  • Opportunities to be part of a TOP 10 CRO and working on Secondment for a TOP Pharma company

  • working to their processes, SOPs and on their systems.

  • Competitive compensation package

  • Opportunities to further develop data management project management and oversight skills and experience.

Please note that we can not support with Visa / Work Permit sponsorship's

  • hence only those applicants that are authorized to work in any of the above European countries can be considered.

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