Associate Clinical Research Coordinator

Mayo Clinic • Phoenix, AZ

5d

About The Position

Are you interested in a position that provides career development and growth? How about a position that is multifaceted, rewarding, and where the learning never stops? If so, then Mayo Clinic invites you to consider a life-changing career as an Associate Clinical Research Coordinator. As an Associate Clinical Research Coordinator, you will have the opportunity to work with a variety of people, from patients to care teams, enabling you to be a part of the legacy that puts the needs of the patients first. As an Associate Clinical Research Coordinator, you will: 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 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 reports appropriately. Collect, abstract, and enter research data. Perform administrative and regulatory duties related to the study as assigned. Participate in other protocol development activities and executes other assignments as warranted and assigned. Please note that Visa Sponsorship is not available for this role. Mayo Clinic does not participate in the OPT Stem program.

Requirements

• Must meet one of the following:
• HS Diploma with at least 3 years of experience
• Associate's degree/college Diploma/Certificate Program with at least 1 year of experience
• Associate’s in Clinical Research from an accredited academic institution without experience
• Bachelor's degree
• Experience should be in the clinical setting or related field
• Visa sponsorship is not available for this position.
• This position is not eligible for F-1 OPT STEM extension.
• Internal candidates are encouraged to attach their performance appraisals (1-3), if available.

Nice To Haves

• Graduate or diploma from a study coordinator training program is preferred.
• One year of clinical research experience is preferred.
• Medical terminology course is preferred.

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.
• May assist in complex 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 reports appropriately.
• Collect, abstract, and enter research data.
• Perform administrative and regulatory duties related to the study as assigned.
• Participate in other protocol development activities and executes other assignments as warranted and assigned.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED
• Number of Employees: 5,001-10,000 employees