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Introduction to Clinical Data Management for Clinical Researchers

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No sessions planned as this time, however if you are interested in taking this course please contact us at info@eccrt.com
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About this course

Reasons to attend

This course provides you with the clinical data management fundamentals that will allow you to become familiar with the key words & terminology, the associated regulations and the processes used in Clinical Data Management.

What's included?

  • Documents and materials related to this course are included
  • Globally recognised certificates awarded after test completion
  • This course has been granted PharmaTrain Recognition

Course schedule

  • One Day face-to-face training: 09h00-17h00


Course Description


Clinical Data Management is one of the Clinical Trial components the most often outsourced to CROs. As such the role of the Clinical Researcher (Clinical project manager, Study lead, Clinical Trial Physician, etc.) is to oversee the expected deliverables of CROs involved in their data management activities.

In that role, you will have to understand the basics of Clinical Data Management vocabulary, concepts, workflow and roles. This course provides you with the fundamentals that will allow you to become familiar with the key words, the associated regulations and the processes used in Data Management.

After this 1-Day course you will never ask yourself about what means a DMP, a DVP, a DB Lock, an eCRF, an Edit Check, CDISC SDTM, Data Transfer and reconciliation, Data Cleaning, etc.

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