University of California, Davis
Assistant Clinical Research Coordinator/ Clinical Research Coordinator
University of California, Davis, Sacramento, California, United States, 95828
Assistant Clinical Research Coordinator / Clinical Research Coordinator
Join the University of California, Davis Cancer Center to support low‑to‑medium complexity cancer‑related clinical research protocols. The role is performed under the direct supervision of the Clinical Research Supervisor.
Key Responsibilities
40% Study Management – protocol development, site monitoring and coordination.
40% Data Coordination – data entry, source data verification and database maintenance.
15% Quality Assurance – GCP compliance audits, SOP reviews and audit preparation.
5% Other – regulatory documentation, sponsor communication and attendance at research team meetings.
Minimum Qualifications
Minimum 1 year relevant experience in clinical research.
Knowledge of disease processes, basic anatomy, medical terminology and interpretation of physician notes.
Familiarity with FDA, OHRP and other clinical research regulations.
Working knowledge of Microsoft Office Suite (Word, Excel, Outlook, Access).
Strong recordkeeping, analytical, organizational and writing skills.
Ability to work occasional overtime and travel on occasion.
High school diploma, GED equivalent or sufficient experience to perform duties.
Minimum 2 years of experience coordinating clinical trials.
Bachelor’s degree in a related area.
Previous oncology‑related clinical research experience preferred.
Preferred Qualifications
Certification by SoCRA or ACRP.
Knowledge of regulatory processes and data management activities in clinical trial coordination.
Demonstrates good judgment and critical thinking skills.
Knowledge and understanding of disease processes as applied to human clinical research.
Salary and Benefits Assistant CRC: $29.02 - $46.72 per hour; CRC: $32.01 - $51.48 per hour. Benefits include comprehensive health, dental and vision coverage, paid holidays, paid time off, continuing education allowance, work‑life wellness programs, employee assistance, retirement savings, loan forgiveness and other standard UC Davis benefits.
Physical Demands
Occasional overtime and travel on occasion.
Lifting 26-50 lbs occasionally; standing, walking and sitting for extended periods.
Reaching overhead and keyboard use occasionally.
Frequent noise levels, chemicals and dust exposure as part of the research environment.
Work Environment
UC Davis campus is smoke and tobacco free.
Position is critical—requires background check, drug screening, medical evaluation and functional capacity assessment.
Mandatory reporter under CANRA and UC policy; compliance with training and reporting requirements required.
EEO Statement UC Davis is an Equal Opportunity Employer. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age or protected veteran status.
#J-18808-Ljbffr
Key Responsibilities
40% Study Management – protocol development, site monitoring and coordination.
40% Data Coordination – data entry, source data verification and database maintenance.
15% Quality Assurance – GCP compliance audits, SOP reviews and audit preparation.
5% Other – regulatory documentation, sponsor communication and attendance at research team meetings.
Minimum Qualifications
Minimum 1 year relevant experience in clinical research.
Knowledge of disease processes, basic anatomy, medical terminology and interpretation of physician notes.
Familiarity with FDA, OHRP and other clinical research regulations.
Working knowledge of Microsoft Office Suite (Word, Excel, Outlook, Access).
Strong recordkeeping, analytical, organizational and writing skills.
Ability to work occasional overtime and travel on occasion.
High school diploma, GED equivalent or sufficient experience to perform duties.
Minimum 2 years of experience coordinating clinical trials.
Bachelor’s degree in a related area.
Previous oncology‑related clinical research experience preferred.
Preferred Qualifications
Certification by SoCRA or ACRP.
Knowledge of regulatory processes and data management activities in clinical trial coordination.
Demonstrates good judgment and critical thinking skills.
Knowledge and understanding of disease processes as applied to human clinical research.
Salary and Benefits Assistant CRC: $29.02 - $46.72 per hour; CRC: $32.01 - $51.48 per hour. Benefits include comprehensive health, dental and vision coverage, paid holidays, paid time off, continuing education allowance, work‑life wellness programs, employee assistance, retirement savings, loan forgiveness and other standard UC Davis benefits.
Physical Demands
Occasional overtime and travel on occasion.
Lifting 26-50 lbs occasionally; standing, walking and sitting for extended periods.
Reaching overhead and keyboard use occasionally.
Frequent noise levels, chemicals and dust exposure as part of the research environment.
Work Environment
UC Davis campus is smoke and tobacco free.
Position is critical—requires background check, drug screening, medical evaluation and functional capacity assessment.
Mandatory reporter under CANRA and UC policy; compliance with training and reporting requirements required.
EEO Statement UC Davis is an Equal Opportunity Employer. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age or protected veteran status.
#J-18808-Ljbffr