Know about research study processes including submissions requirements by both IRB and/ or regulatory authorities, protocol requirements to assess potential challenges of the study, and rationale/ purpose of each essential document filed in the investigator site file.
Know about research study processes including submissions requirements by both IRB and/ or regulatory authorities, protocol requirements to assess potential challenges of the study, and rationale/ purpose of each essential document filed in the investigator site file.
Assists PI in designing and development of study recruitment advertisement, study specific source documents/ Case Report Forms and other required documents pertaining to the protocol.
Communicate with study participants to clarify their responsibilities, conduct interviews to identify adverse events, and monitor adherence to study protocols and prescribed medication.
Communicate with study participants to clarify their responsibilities, conduct interviews to identify adverse events, and monitor adherence to study protocols and prescribed medication.