Clinical Research Coordinator – Comprehensive Cancer Center

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🔥 49 minutes ago

🏈 Ohio – Remote

🏈 Ohio – Remote

⏰ Full Time

🟢 Junior

🧪 Clinical Research

👻 Ghost score 13%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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The Ohio State University, Main Campus

WebsiteLinkedInAll Job Openings

1 - 10 employees

Founded 1870

📚 Education

Education

The Ohio State University, Main Campus is a public research university located in Columbus, Ohio. It offers a comprehensive education with a wide array of undergraduate, graduate, and professional programs. The university is engaged in numerous research initiatives and partnerships, providing opportunities for students, faculty, and industry partners to collaborate. Ohio State promotes a vibrant student life with various academic, recreational, and wellness services to support student needs. It also emphasizes community involvement and leadership development, fostering an inclusive environment on its multiple campuses across Ohio.

📋 Description

• 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

• 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

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