Screen study participants per regulatory guidelines
Conduct informed consent discussions with patients
Monitor patient progress and collect trial data
The role involves screening study participants in accordance with regulatory guidelines and ethical standards while conducting informed consent discussions
Job Summary
The role involves screening study participants in accordance with regulatory guidelines and ethical standards while conducting informed consent discussions.
Candidates will monitor patient progress, collect accurate data during clinical trials, and administer study-related interventions as per protocol.
The position offers flexible scheduling with the ability to choose days and provides on-job training for the research field.
Matching Summary
Match Score: 75
The role involves screening study participants in accordance with regulatory guidelines and ethical standards while conducting informed consent discussions.
Salary
Hourly: $30; Schedule: Part-time (3-4 days/week); Benefits: On-job training provided
Skills & Requirements
Must-have
Screen study participants per regulatory guidelines
Conduct informed consent discussions with patients
Monitor patient progress and collect trial data
Administer study-related interventions and medications