Associate Clinical Research Coordinator - Gastroenterology and Hepatology - Limited Tenure

Mayo Clinic•Rochester, MN

About The Position

As an Associate Clinical Research Coordinator, you: Coordinate non-therapeutic (i.e. minimal risk, survey, chart review) clinical research protocols with direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines. May assist in complex (i.e. interventional, therapeutic, greater than minimal risk) studies with direction but does not have overall responsibility for these studies. Screen, enroll, and recruit research participants. Coordinate schedules and monitor research activities and subject participation. Recognize adverse events, protocol deviations, and other unanticipated problems and report appropriately. Collect, abstract, and enter research data. Perform administrative and regulatory duties related to the study as assigned. May be required to do some travel. Participate in Protocol Development and Maintenance Activities Responsibilities, which may include, but are not limited to: ongoing management of the protocol document and process through editing, amendments, proofing, coordination of study logistics (i.e. data collection booklets, use of CRU, etc.), and verification of content to meet institutional and federal standards; Institutional Review Board (IRB) submission; and communication with study sites and/or federal agencies regarding study status changes. Participate in other protocol development activities and execute other assignments as warranted and assigned. During the selection process you may participate in an OnDemand (pre-recorded) interview that you can complete at your convenience. During the OnDemand interview, a question will appear on your screen, and you will have time to consider each question before responding. You will have the opportunity to re-record your answer to each question – Mayo Clinic will only see the final recording. The complete interview will be reviewed by a Mayo Clinic staff member and you will be notified of next steps. This is a limited tenure position with an anticipated duration of up to two years, that may have the possibility of turning into a regular status position. Visa sponsorship is not available for this position. This position is not eligible for F-1 OPT STEM extension.

Responsibilities

Coordinate non-therapeutic (i.e. minimal risk, survey, chart review) clinical research protocols with direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines.
Assist in complex (i.e. interventional, therapeutic, greater than minimal risk) studies with direction but does not have overall responsibility for these studies.
Screen, enroll, and recruit research participants.
Coordinate schedules and monitor research activities and subject participation.
Recognize adverse events, protocol deviations, and other unanticipated problems and report appropriately.
Collect, abstract, and enter research data.
Perform administrative and regulatory duties related to the study as assigned.
May be required to do some travel.
Participate in Protocol Development and Maintenance Activities Responsibilities, which may include, but are not limited to: ongoing management of the protocol document and process through editing, amendments, proofing, coordination of study logistics (i.e. data collection booklets, use of CRU, etc.), and verification of content to meet institutional and federal standards; Institutional Review Board (IRB) submission; and communication with study sites and/or federal agencies regarding study status changes.
Participate in other protocol development activities and execute other assignments as warranted and assigned.