University of Cincinnati
Clinical Research Professional / Clinical Research Professional II, UC Cancer Ce
University of Cincinnati, Cincinnati, Ohio, United States, 45208
Job Title:
Clinical Research Professional / Clinical Research Professional II, UC Cancer Center, Biorepository
Posting Date:
11/4/2025
Work Arrangement:
Full-time, 8:00-4:30 pm onsite with occasional additional hours.
Job Overview The UC Cancer Center Biospecimen Shared Resource (BSR) and Clinical Trial Office (CTO) Lab seeks a full‑time Clinical Research Professional (or Clinical Research Professional II) to screen and enroll eligible patients, collect, process, store, dispense and ship high‑quality human biospecimens in accordance with established BSR and CTO lab procedures.
Essential Functions
Collaborate with medical professionals and investigators to plan and coordinate collection of human biospecimens for research.
Screen and enroll eligible patients to research studies via informed consent.
Collectly record samples and associated health information in the biospecimen management software.
Process, store and ship samples following established procedures.
Complete sample processing documentation and enter chain of custody documentation.
Support laboratory administrative duties through meticulous record keeping and documentation maintenance.
Maintain regulatory documentation; assist with IRB submissions, draft subject informed consents and advertising for research studies.
Operate laboratory equipment and perform routine maintenance and supply inventory.
Assist with research project planning, including project design, cohort identification, data collection and dispensing of biospecimens.
Coordinate data generation for proposals, reports and manuscripts; assist in report development.
Be willing to work after hours and weekends as needed.
Minimum Requirements Clinical Research Professional
Bachelor’s Degree in a related field or equivalently 5 years of relevant work experience/training.
At least 1 year of related experience.
Clinical Research Professional II
Bachelor’s Degree in a related field or equivalently 7 years of relevant work experience/training.
At least 3 years of related experience.
Additional Qualifications Considered
Minimum of one year laboratory experience; knowledge of human subjects research clinical trials and handling of human biospecimens.
Self‑motivated, problem‑solving, independent work style; comfortable interacting with medical professionals and patients.
Strong written and verbal communication skills, including proficiency with Microsoft Excel.
Physical Requirements / Work Environment Office environment—no specific unusual physical or environmental demands.
Compensation and Benefits UC offers an exceptional benefits package, including tuition remission, robust retirement plans, generous paid time off (vacation, sick time, 11 paid holidays, 6 weeks parental leave), competitive salary, comprehensive health coverage, flexible spending accounts, wellness programs and professional development opportunities.
To learn more about UC’s benefits, visit https://www.uc.edu/careers.html.
UC is an E‑Verify employer. Accepted employment‑eligibility documents are available at https://www.uscis.gov/i-9-central/form-i-9-acceptable-documents.
Equal Opportunity Employer. Building a workplace where all qualified applicants will receive consideration for employment, including Individuals with Disabilities and Protected Veterans.
REQ:100390
SF:OMJ SF:RM SF:HEJ, SF:INS SF:HERC SF:DIV SF:LJN SF:IHE
#J-18808-Ljbffr
Clinical Research Professional / Clinical Research Professional II, UC Cancer Center, Biorepository
Posting Date:
11/4/2025
Work Arrangement:
Full-time, 8:00-4:30 pm onsite with occasional additional hours.
Job Overview The UC Cancer Center Biospecimen Shared Resource (BSR) and Clinical Trial Office (CTO) Lab seeks a full‑time Clinical Research Professional (or Clinical Research Professional II) to screen and enroll eligible patients, collect, process, store, dispense and ship high‑quality human biospecimens in accordance with established BSR and CTO lab procedures.
Essential Functions
Collaborate with medical professionals and investigators to plan and coordinate collection of human biospecimens for research.
Screen and enroll eligible patients to research studies via informed consent.
Collectly record samples and associated health information in the biospecimen management software.
Process, store and ship samples following established procedures.
Complete sample processing documentation and enter chain of custody documentation.
Support laboratory administrative duties through meticulous record keeping and documentation maintenance.
Maintain regulatory documentation; assist with IRB submissions, draft subject informed consents and advertising for research studies.
Operate laboratory equipment and perform routine maintenance and supply inventory.
Assist with research project planning, including project design, cohort identification, data collection and dispensing of biospecimens.
Coordinate data generation for proposals, reports and manuscripts; assist in report development.
Be willing to work after hours and weekends as needed.
Minimum Requirements Clinical Research Professional
Bachelor’s Degree in a related field or equivalently 5 years of relevant work experience/training.
At least 1 year of related experience.
Clinical Research Professional II
Bachelor’s Degree in a related field or equivalently 7 years of relevant work experience/training.
At least 3 years of related experience.
Additional Qualifications Considered
Minimum of one year laboratory experience; knowledge of human subjects research clinical trials and handling of human biospecimens.
Self‑motivated, problem‑solving, independent work style; comfortable interacting with medical professionals and patients.
Strong written and verbal communication skills, including proficiency with Microsoft Excel.
Physical Requirements / Work Environment Office environment—no specific unusual physical or environmental demands.
Compensation and Benefits UC offers an exceptional benefits package, including tuition remission, robust retirement plans, generous paid time off (vacation, sick time, 11 paid holidays, 6 weeks parental leave), competitive salary, comprehensive health coverage, flexible spending accounts, wellness programs and professional development opportunities.
To learn more about UC’s benefits, visit https://www.uc.edu/careers.html.
UC is an E‑Verify employer. Accepted employment‑eligibility documents are available at https://www.uscis.gov/i-9-central/form-i-9-acceptable-documents.
Equal Opportunity Employer. Building a workplace where all qualified applicants will receive consideration for employment, including Individuals with Disabilities and Protected Veterans.
REQ:100390
SF:OMJ SF:RM SF:HEJ, SF:INS SF:HERC SF:DIV SF:LJN SF:IHE
#J-18808-Ljbffr