Clinical Research Coordinator – Comprehensive Cancer Center

The Ohio State University, Main Campus

. Coordinate multiple clinical, population-based, and community-engaged research studies .

Posted 10/16/2026full-timeRemote • Ohio • United StatesJuniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in coordinating clinical and community-engaged research studies while ensuring compliance with regulatory requirements and maintaining effective stakeholder relationships. Proficient in data management and participant tracking using electronic data capture systems.

Highest-signal resume keywords

Clinical Research CoordinationGood Clinical Practice (GCP)Electronic Data Capture SystemsRegulatory ComplianceStakeholder Engagement

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Data CollectionParticipant RecruitmentStudy Protocol ImplementationQuality Assurance ProceduresData Management

Soft Skills

CommunicationRelationship BuildingProblem SolvingOrganizational Skills

Tools & Technologies

Study DatabasesParticipant Tracking Systems

Industry Keywords

Federal RegulationsHIPAAInstitutional Review Board (IRB)Community Health EngagementPopulation-Based Research

About the role

Key responsibilities & impact

Coordinate multiple clinical, population-based, and community-engaged research studies
Implement study protocols and standard operating procedures in accordance with sponsor, institutional, and regulatory requirements
Oversee participant recruitment, enrollment, informed consent, data collection, and follow-up activities
Schedule and conduct study visits in clinical, community, and virtual settings
Maintain study databases and participant tracking systems
Assist investigators with study startup, activation, and closeout activities
Monitor study progress and ensure adherence to project timelines and deliverables
Serve as primary liaison between research teams and community partners across rural Ohio
Build and maintain relationships with healthcare organizations, community health centers, faith-based organizations, local health departments, and other stakeholders
Coordinate outreach events, educational programs, health fairs, screening initiatives, and community meetings
Develop and implement culturally appropriate recruitment and retention strategies
Support Community Advisory Boards and stakeholder engagement activities
Facilitate participant navigation and address barriers to study participation
Prepare and submit Institutional Review Board (IRB) applications, amendments, continuing reviews, and reportable events
Maintain regulatory binders and study documentation
Ensure compliance with federal regulations, Good Clinical Practice (GCP), HIPAA, and university policies
Participate in study monitoring visits, audits, and sponsor reviews
Track protocol deviations and assist with corrective action plans
Collect, enter, verify, and manage research data using electronic data capture systems
Perform quality assurance and quality control procedures
Generate reports for investigators, sponsors, and project leadership
Assist with abstracts, manuscripts, presentations, and progress reports
Support dissemination of research findings to community and academic audiences
Participate in project meetings, training activities, and professional development
Assist with supervision and training of student employees and research assistants
Perform additional duties as assigned to support research program objectives

Requirements

What you’ll need

Bachelor’s Degree in Biological Sciences, Health Sciences, Social Sciences or another medical field, or equivalent combination of education and experience required
1 year of relevant experience required
2–4 years of relevant experience preferred
Frequent travel throughout rural Ohio is required
Successful completion of a background check required for final candidates
Drug screen or physical may be required during the post-offer process
Knowledge of sponsor, institutional, and regulatory requirements
Knowledge of federal regulations, Good Clinical Practice (GCP), HIPAA, and university policies
Ability to coordinate clinical, population-based, and community-engaged research studies
Ability to use electronic data capture systems and maintain study databases

Benefits

Comp & perks

Full-time schedule of 40 hours per week
Regular position
Remote work arrangement
Professional development opportunities
Equal opportunity employment, including veterans and disability