Research Associate

7 days ago


Bloemfontein, Orange Free State, South Africa IQVIA Full time

Job Purpose

The Clinical Data Associate will be responsible for managing freeze / lock of eCRF, file documentation in the virtual Trial Master File (TMF), and receives and enters lab normal ranges.

Responsibilities

  • Manage freeze / lock of eCRF.
  • File documentation in the virtual Trial Master File (TMF).
  • Receives and enters lab normal ranges.
  • 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.


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