Clinical Research Coordinator - Comprehensive Cancer Center
Listed on 2026-01-20
-
Healthcare
Clinical Research -
Research/Development
Clinical Research
Job Title and Department
Clinical Research Coordinator - Comprehensive Cancer Center Department: CCC | Sponsored Research
Position SummaryThe Clinical Research Coordinator plays a crucial role in coordinating daily activities and efforts related to the Center for Cancer Prevention and Survivorship. The individual will primarily focus on facilitating clinical research projects in areas such as cancer prevention and control and dietary and physical activity interventions.
Responsibilities- Assist with research projects, such as participant recruitment, informed consent, scheduling, assessments, data collection, monitor and document adverse events to behavioral intervention
- Assist with behavioral intervention development and delivery
- Assist with developing and managing regulatory protocols. Support activities to ensure compliance with all Institutional Review Boards (IRB), federal, state, and industry sponsor regulations
- Assist with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors
- Assist with collaborations within and across departments to develop new research projects
- Conducts scientific literature reviews, systematic reviews, and assists in drafting manuscripts, analyzing relevant research to support the development of scientific publications
- Performs accurate medical chart reviews and data abstraction from EHRs, ensuring meticulous record-keeping in accordance with established protocols
- Attends study meetings and provides regular updates on study progress
- Submission (not writing) of scientific manuscripts
- Excellent communication and writing skills
- Highly organized and self-driven
Bachelor’s Degree in Biological Sciences, Health Sciences, Social Sciences or other medical field, or equivalent combination of education experience required. 1 year of relevant experience required.
Additional InformationResearch and Scholarship - Clinical Research - Individual Contributor - Specialized - S2
Location and Position TypeLocation:
Olentangy River Rd, 3650 (2520)
Position Type:
Regular
Scheduled
Hours:
40
Shift: First Shift
Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.
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EqualOpportunity
The university is an equal opportunity employer, including veterans and disability.
As required by Ohio Revised Code section , Ohio State will: educate students by means of free, open and rigorous intellectual inquiry to seek the truth; equip students with the opportunity to develop intellectual skills to reach their own, informed conclusions; not require, favor, disfavor or prohibit speech or lawful assembly; create a community dedicated to an ethic of civil and free inquiry, which respects the autonomy of each member, supports individual capacities for growth and tolerates differences in opinion;
treat all faculty, staff and students as individuals, hold them to equal standards and provide equality of opportunity with regard to race, ethnicity, religion, sex, sexual orientation, gender identity or gender expression.
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