Clinical Research Coordinator: Lead Interventional Trials

Mayo Foundation for Medical Education and Research; Phoenix (AZ); On-site; USD 66,000 - 98,000; Full time

Benefits offered by this job

Medical plans

Dental coverage

Vision plan

HSA/FSAs

Retirement plan

Job summary

Mayo Clinic is seeking a Clinical Research Coordinator to independently manage complex interventional protocols in a compliant, patient-centered environment. You will collaborate with investigators, staff, and study sites to ensure protocol execution and data quality.

The role includes screening and enrolling participants, reporting adverse events, and coordinating regulatory tasks. The position may require some travel and offers a comprehensive benefits package.

Qualifications

• HS Diploma with at least 5 years of clinical research coordination/related experience.
• Associate's degree/college Diploma/Certificate Program with at least 3 years of experience, Associate's in Clinical Research from an accredited academic institution without experience OR Bachelor's with at least 1 year of experience or Mayo Clinic-sponsored clinical research internship in lieu of 1 year of experience.
• 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

• Independently coordinates complex clinical research protocols with minimal direction from the principal investigator.
• Collaborates with study team to manage feasibility and protocol execution.
• Screens, enrolls, and recruits research participants and coordinates schedules.
• Identifies, reviews, and reports adverse events and protocol deviations.
• Manages data and regulatory duties to ensure quality and compliance.

Skills

Clinical research coordination

Regulatory knowledge

Medical terminology

Education

HS Diploma

Associate's degree / certificate

Bachelor's degree

Mayo Clinic internship

Job description

Mayo Clinic is seeking a Clinical Research Coordinator to independently manage complex interventional protocols in a compliant, patient-centered environment. You will collaborate with investigators, staff, and study sites to ensure protocol execution and data quality.

The role includes screening and enrolling participants, reporting adverse events, and coordinating regulatory tasks. The position may require some travel and offers a comprehensive benefits package.