Clinical Research Coordinator — Complex Trials & Compliance

Mayo Clinic; Eau Claire (WI); Hybrid; USD 39,000 - 58,000; Full time

Benefits offered by this job

Benefits Eligible

Job summary

Mayo Clinic is seeking a skilled Clinical Research Coordinator to independently coordinate complex protocols under minimal direction and in compliance with regulatory standards.

You will collaborate with the team to assess feasibility, enroll and monitor participants, and ensure protocol adherence from IRB approval through final reports. Some travel may be required, with education provided within an established Mayo Clinic research environment.

Qualifications

• 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.
• Bachelor's with at least 1 year of experience or Mayo Clinic-sponsored internship in lieu of 1 year.
• Experience should be in clinical setting or related experience.

Responsibilities

• Coordinates complex clinical research protocols with minimal direction.
• Collaborates with research team to assess feasibility and management.
• Ensures protocol implementation after IRB approval and provides information for progress reports.
• Screens, enrolls, and recruits research participants.
• Identifies, reviews, and reports adverse events and protocol deviations.
• Manages, monitors, and reports data to maintain quality and compliance.
• Provides education/training for others within the department.
• Performs administrative/regulatory duties related to the study.
• Some travel may be required.
• Communication with study sites and federal agencies regarding study status.

Skills

Clinical research

Regulatory knowledge

IRB familiarity

Data management

SOP adherence

Education

HS Diploma

Associate’s degree

Bachelor's degree

Clinical research internship

Job description

Mayo Clinic is seeking a skilled Clinical Research Coordinator to independently coordinate complex protocols under minimal direction and in compliance with regulatory standards.

You will collaborate with the team to assess feasibility, enroll and monitor participants, and ensure protocol adherence from IRB approval through final reports. Some travel may be required, with education provided within an established Mayo Clinic research environment.