Sr. Clinical Research Coordinator
About the role
This position will coordinate multiple research studies and clinical trials under the clinical direction of each study's Principal Investigator (PI) and the operational direction of the Manager of Clinical Studies. The role assists the PI in recruiting and retaining study subjects by obtaining informed consents, screening patients, and maintaining research records and files. It guides the day-to-day operations of each assigned study, ensuring adherence to protocol, accuracy of reports, and timely resolution of queries. The position also monitors agency, sponsor, and contracted vendors in cooperation with the UB Clinical Research Office (CRO).
Responsibilities
- Coordinate multiple research studies and clinical trials.
- Assist Principal Investigators (PIs) in recruitment and retention of study subjects.
- Obtain informed consents and screen patients.
- Maintain research records and files.
- Guide day-to-day operations of assigned studies, ensuring adherence to protocol.
- Ensure accuracy of reports and timely resolution of queries.
- Monitor agency, sponsor, and contracted vendors in cooperation with the UB Clinical Research Office (CRO).
Requirements
- Bachelor's degree in science or healthcare-related field.
- 3 years of clinical research experience.
Working Conditions
- Essential weight requirement: Sedentary (10 lbs).
Schedule
- Full-time, bi-weekly standard hours: 75.00.
- Scheduled work hours: 8:00 AM – 4:00 PM.
- No weekend or holiday requirement.
- No on-call required.
- Hybrid work arrangement.
Pay
Salary range: $58,666.92 – $80,674.62. Wage will be determined based on factors such as candidate's experience, qualifications, internal equity, and any applicable collective bargaining agreement. Pay frequency: bi-weekly.