Research Associate
7 days ago
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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