Clinical Research Coordinator

Clinical Research Coordinator University of Missouri-Columbia parental leave, paid time off United States, Missouri, Columbia 801 Conley Avenue (Show on map) Mar 05, 2026 Hiring Department Department of Radiology Job Description Position Summary The Clinical Research Coordinator is responsible for the day-to-day management and execution of clinical research studies and protocols. This position oversees participant recruitment and enrollment, regulatory compliance, study implementation, data collection, and coordination of protocol requirements. The Coordinator works closely with the Principal Investigator (PI), research team, clinical staff, and sponsoring agencies to ensure studies are conducted in accordance with institutional, federal, and regulatory guidelines. ________________________________________ Key Responsibilities Participant Recruitment & Enrollment

• Recruit, screen, and enroll study participants in accordance with protocol eligibility criteria.
• Determine participant eligibility through diagnostic criteria, interviews, observations, and data analysis.
• Develop informed consent packets and conduct consent discussions with participants and families.
• Explain study purpose, diagnostic procedures, and treatment plans to address participant and family concerns.
• Administer and score required assessments and ensure completion of all clinical and laboratory evaluations. Study & Protocol Management
• Implement and manage all phases of assigned studies and research protocols.
• Ensure strict compliance with study guidelines and regulatory agency requirements.
• Establish and maintain accurate record-keeping systems.
• Monitor participant progress and assess outcomes throughout study participation.
• Analyze, investigate, and report adverse events in accordance with regulatory requirements.
• Determine when physician notification is required, when participant inclusion should be paused or stopped, and when protocol adjustments may be necessary.
• Resolve IRB and protocol management issues and recommend corrective actions as needed.
• Serve as liaison between the research team and funding/sponsoring agencies. Clinical & Data Responsibilities
• Ensure timely completion of all protocol requirements including assessments, lab testing, procedures, and treatments.
• Schedule and coordinate participant visits to maintain protocol compliance.
• Collect and process research specimens in accordance with environmental health and safety standards.
• Perform study-required procedures such as vital signs, specimen collection, and processing (training provided as needed).
• Review research supply inventory and monitor expiration dates regularly.
• Evaluate and interpret clinical data in collaboration with the PI.
• Prepare written reports, analyses, and presentations summarizing study progress, trends, and recommendations. Regulatory Compliance
• Create, maintain, and update regulatory documentation to ensure full compliance.
• Prepare and submit IRB applications, amendments, personnel change forms, and continuing review reports.
• Complete required clinical trial regulatory documents.
• Ensure adherence to HIPAA policies and institutional research standards.
• Maintain current Institutional and CITI training certifications.
• Acquire and apply knowledge of institutional, state, and federal research regulations and guidelines. Collaboration & Professional Conduct
• Foster a positive, efficient, and professional research environment.
• Communicate and collaborate consistently with clinic personnel, departmental leadership, and research teams.
• Contribute to team initiatives and process improvements. Additional Responsibilities
• Perform other duties as assigned. Shift Monday
• Friday 8:00 a.m.
• 5:00 p.

m. Minimum Qualifications A Bachelor's degree or an equivalent combination of education and relevant experience and at least 3 years of experience from which comparable knowledge and skills can be acquired is necessary.

Anticipated Hiring Range Salary Range:

$55,000

• $75,000 annually

Grade:

GGS

• 010

University Title:

RESEARCH CONSULTANT

Internal applicants can determine their university title by accessing the Talent Profile tile in myHR. Application Materials In addition to the Online Application, please provide a Cover Letter and Resume. Community Information Columbia offers small-town friendliness with big city features and a high quality of life for people of all ages and interests. Founded on education and known as an ideal college town, its location also makes it an attractive spot for businesses and travelers. Located on Interstate 70 and U.S. Highway 63, Columbia is right in the middle of the state and the nation. Just a couple hours' drive from St. Louis and Kansas City, Columbia is Boone County's largest population center offering big-city culture, activities, and resources with a low cost of living. Columbia is home to a variety of restaurants and entertainment venues and hosts more than a dozen festivals each year. If you want to grow your career, continue your education, raise a family, and retire, Columbia is a good place to be! Benefit Eligibility This position is eligible for University benefits. As part of your total compensation, the University offers a comprehensive benefits package, including medical, dental and vision plans, retirement, paid time off, short

• and long-term disability, paid parental leave, paid caregiver leave, and educational fee discounts for all four UM System campuses.

For additional information on University benefits, please visit the Faculty & Staff Benefits website at https://www.umsystem.edu/totalrewards/benefits. Equal Employment Opportunity The University of Missouri is an Equal Opportunity Employer. To request ADA accommodations, please call the Director of Accessibility and ADA at 573-884-7278.