The role serves as a virtual study coordinator for Principal Investigators and patients participating in pregnancy registries and observational trials
Job Summary
The role serves as a virtual study coordinator for Principal Investigators and patients participating in pregnancy registries and observational trials.
Responsibilities include administering informed consent, collecting data in electronic systems, and escalating adverse events according to protocol.
Candidates must possess a BSN with at least two years of experience and working knowledge of Good Clinical Practice principles.
Matching Summary
The role serves as a virtual study coordinator for Principal Investigators and patients participating in pregnancy registries and observational trials.