Clinical Research Coordinator

6 days ago


Bloemfontein, Orange Free State, South Africa IQVIA Full time

Job Summary

The Clinical Data Associate will be responsible for performing comprehensive data management tasks, including data review, query generation and resolution. This role will also involve creating eCRF completion guidelines, entering test data, testing data validation rules, and performing study closeout/Archiving activities.

Responsibilities

  • Perform data management tasks, including data review, query generation and resolution.
  • Create eCRF completion guidelines.
  • Enter test data for eCRF and the Data Review Model.
  • Test data validation rules.
  • Perform study closeout/Archiving activities.
  • Attend study-related meetings/teleconferences.

Requirements

  • Bachelor's degree in a Health or Science discipline with experience in clinical research.
  • Data Management experience and experience working on a clinical trial mandatory.
  • Rave experience mandatory.
  • Experience working in highly diverse teams within clinical research; cross-functional, global, multi-regional.
  • Knowledge of current industry standards (e.g., CDISC, SDTM, CDASH, etc.)


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