Clinical Research Coordinator

Mayo Clinic • Phoenix, AZ

409d • $62,650 - $93,995

About The Position

The Clinical Research Coordinator at Mayo Clinic is responsible for independently coordinating complex clinical research protocols with minimal direction. This role involves collaborating with various departments, managing research data, and ensuring compliance with regulatory laws and institutional guidelines. The position requires interaction with research participants and other stakeholders to facilitate the efficient completion of research studies.

Requirements

• HS Diploma with at least 5 years of clinical research coordination/related experience OR Associate's degree with at least 3 years of experience OR Bachelor's with at least 1 year of experience or completion of a Mayo Clinic-sponsored clinical research internship in lieu of 1 year of experience.
• Experience in a clinical setting or related experience is required.

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

• Receives direction from principal investigator, supervisor, or other staff involved in research protocol(s).
• Gives direction to and works cooperatively with other research staff.
• Collaborates with various departments within the institution.
• Interacts with research participants, other research centers, and sponsoring companies to resolve problems and ensure efficient completion of research studies.
• Independently coordinates complex clinical research protocols in compliance with regulatory laws and institutional guidelines.
• Collaborates with research team to assess feasibility and management of research protocols.
• Ensures implementation of research protocols after IRB approval and provides information for progress reports.
• Screens, enrolls, and recruits research participants.
• Coordinates schedules and monitors research activities and subject participation.
• Identifies, reviews, and reports adverse events, protocol deviations, and other unanticipated problems appropriately.
• Manages, monitors, and reports research data to maintain quality and compliance.
• Provides education/training for others within the department.
• Performs administrative and regulatory duties related to the study as appropriate.

Benefits

• Competitive compensation
• Comprehensive benefit plans
• Continuing education and advancement opportunities

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Hospitals
• Education Level: High school or GED