Clinical Research Professional/Clinical Research Professional II, UC Cancer Cent
Inside Higher Ed, Cincinnati, OH, United States
Job Overview
Recruitment for a Clinical Research Professional or Clinical Research Professional II supporting the University of Cincinnati Cancer Center Clinical Trials Office (CTO). Responsibilities span clinical trials workflow, patient coordination, data documentation, specimen collection, financial documentation, and stakeholder collaboration.
Essential Functions
Follow established CTO workflows and standard operating procedures.
Consent participants to interventional clinical trials and coordinate screening procedure scheduling and completion.
Complete eligibility review and verification with treating physician/sub‑I and CRC team.
Coordinate treatment appointments/procedures for patients during study duration.
Document study procedures and patient medical history, concomitant medications, and adverse events in Epic electronic medical record.
Respond to queries in electronic data capture systems and other online study systems as needed.
Prepare biospecimen collection supplies.
Complete ECGs on study‑provided ECG machines.
Coordinate collection, documentation, transportation, and shipment of research biospecimens as needed.
Document and file deviations through the appropriate regulatory channels.
Complete financial documentation for research patient visits.
Prepare and present educational/operational materials.
Create and maintain positive working relationships with multidisciplinary teams.
Perform related duties based on departmental or team needs.
Clinical Research Professional
Required Education: Bachelor’s Degree in a related field.
Required Experience: One (1) year of related experience.
Clinical Research Professional II
Required Education: Bachelor’s Degree in a related field. Five (5) years of relevant work experience and/or specialized training may satisfy the educational requirement.
Required Experience: Seven (7) years of relevant work experience and/or specialized training may satisfy the experience requirement. Three (3) years of related experience is also considered.
Additional Qualifications Considered
Master’s degree.
Experience in an academic or clinical setting in the area of clinical specialization.
Physical Requirements/Work Environment
Office environment; no specific unusual physical or environmental demands.
Compensation And Benefits
Competitive salary based on experience.
Comprehensive health coverage (medical, dental, vision, prescription).
Flexible spending accounts and wellness programs.
Professional development and mentorship opportunities.
Tuition remission for employee and eligible dependents.
Robust retirement plans: choice among state pension plans (OPERS, STRS) or an Alternative Retirement Plan (ARP) with 14‑18% UC contribution.
Generous paid time off: vacation/sick time, 11 paid holidays, additional end‑of‑year paid time off, 6 weeks of paid parental leave.
Equal Opportunity Employer
Building a workplace where all qualified applicants receive consideration for employment, including individuals with disabilities and protected veterans.
REQ: 102131
#J-18808-Ljbffr
Recruitment for a Clinical Research Professional or Clinical Research Professional II supporting the University of Cincinnati Cancer Center Clinical Trials Office (CTO). Responsibilities span clinical trials workflow, patient coordination, data documentation, specimen collection, financial documentation, and stakeholder collaboration.
Essential Functions
Follow established CTO workflows and standard operating procedures.
Consent participants to interventional clinical trials and coordinate screening procedure scheduling and completion.
Complete eligibility review and verification with treating physician/sub‑I and CRC team.
Coordinate treatment appointments/procedures for patients during study duration.
Document study procedures and patient medical history, concomitant medications, and adverse events in Epic electronic medical record.
Respond to queries in electronic data capture systems and other online study systems as needed.
Prepare biospecimen collection supplies.
Complete ECGs on study‑provided ECG machines.
Coordinate collection, documentation, transportation, and shipment of research biospecimens as needed.
Document and file deviations through the appropriate regulatory channels.
Complete financial documentation for research patient visits.
Prepare and present educational/operational materials.
Create and maintain positive working relationships with multidisciplinary teams.
Perform related duties based on departmental or team needs.
Clinical Research Professional
Required Education: Bachelor’s Degree in a related field.
Required Experience: One (1) year of related experience.
Clinical Research Professional II
Required Education: Bachelor’s Degree in a related field. Five (5) years of relevant work experience and/or specialized training may satisfy the educational requirement.
Required Experience: Seven (7) years of relevant work experience and/or specialized training may satisfy the experience requirement. Three (3) years of related experience is also considered.
Additional Qualifications Considered
Master’s degree.
Experience in an academic or clinical setting in the area of clinical specialization.
Physical Requirements/Work Environment
Office environment; no specific unusual physical or environmental demands.
Compensation And Benefits
Competitive salary based on experience.
Comprehensive health coverage (medical, dental, vision, prescription).
Flexible spending accounts and wellness programs.
Professional development and mentorship opportunities.
Tuition remission for employee and eligible dependents.
Robust retirement plans: choice among state pension plans (OPERS, STRS) or an Alternative Retirement Plan (ARP) with 14‑18% UC contribution.
Generous paid time off: vacation/sick time, 11 paid holidays, additional end‑of‑year paid time off, 6 weeks of paid parental leave.
Equal Opportunity Employer
Building a workplace where all qualified applicants receive consideration for employment, including individuals with disabilities and protected veterans.
REQ: 102131
#J-18808-Ljbffr