Overnight Monitor I
Summary
Overnight Study Monitor ensures clinical trial activities run smoothly outside regular hours, completing documentation and reporting data accurately.
The Overnight Study Monitor’s primary purpose is to assist with study operation in the absence of the clinical coordinators. They will ensure overnight study activities occur as scheduled and all associated documents are complete.
- Conduct activities at scheduled times.
- Accurately report study data on source documents.
- Communicate with other staff to provide organized completion of activities.
- Execute other duties as assigned.