University of California - Davis
Assistant Clinical Research Coordinator/ Clinical Research Coordinator
University of California - Davis, Sacramento, California, United States, 95828
Job Summary
Assistant Clinical Research Coordinator (ACRC) supports cancer protocols at the UC Davis Comprehensive Cancer Center under the Clinical Research Supervisor. The ACRC coordinates study management, data coordination, quality assurance, and other trial activities in compliance with Good Clinical Practice (GCP), SOPs, and university policies.
Key Responsibilities
Study Management
– Coordinate protocol-specific activities, patient recruitment, screening, consent, scheduling, and clinical assessments.
Data Coordination
– Maintain accurate data in electronic data capture systems, ensure timely data entry, and resolve data queries.
Quality Assurance
– Conduct audit preparation, prepare study reports, and assist in monitoring visits.
Other
– Liaise with sponsors, governing agencies, IRB, FDA, and research network committees; facilitate communication and documentation.
Qualifications
Minimum 1‑year relevant clinical research experience.
Knowledge of disease processes, basic anatomy, clinical research regulations (FDA, OHRP), and medical terminology.
Proficiency with Microsoft Office Suite (Word, Excel, Outlook, Access).
Tracking, recordkeeping, and analytical skills for data management.
Strong organizational, writing, and communication abilities.
Ability to work occasional overtime and travel on occasion.
HS or GED equivalent and/have demonstrated skills to perform duties.
Minimum 2 years of experience coordinating clinical trials.
Bachelor’s degree in a related area.
Certification by SoCRA or ACRP preferred.
Previous oncology‑related clinical research experience preferred.
Preferred Qualifications
Experience with cancer‑related protocols and on‑core data management.
Experience coordinating Phase I or maintenance clinical trials.
SoCRA or ACRP certification.
Salary Assistant CRC: $29.02–$46.72 per hour. CRC: $32.01–$51.48 per hour. Hourly, 100% full time, Monday‑Friday 8:00‑17:00.
Location & Shift Sacramento, California – Facilities Support Services Building (HSP068). Hybrid – mix of on‑site and remote work.
Benefits Full range of UC Davis benefits: medical, dental, vision, paid holidays, sick leave, PTO, pregnancy & parental leave, retirement, and professional development grants. Union representation: RX‑Research Professionals.
EEO Statement 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.
Application Deadline Apply by 10/25/2025 at 11:59pm.
Important This position is not a H‑1B visa opportunity and does not require a H‑1B visa application.
Contact To apply or learn more, visit the UC Davis Comprehensive Cancer Center job portal or contact your recruiter.
#J-18808-Ljbffr
Key Responsibilities
Study Management
– Coordinate protocol-specific activities, patient recruitment, screening, consent, scheduling, and clinical assessments.
Data Coordination
– Maintain accurate data in electronic data capture systems, ensure timely data entry, and resolve data queries.
Quality Assurance
– Conduct audit preparation, prepare study reports, and assist in monitoring visits.
Other
– Liaise with sponsors, governing agencies, IRB, FDA, and research network committees; facilitate communication and documentation.
Qualifications
Minimum 1‑year relevant clinical research experience.
Knowledge of disease processes, basic anatomy, clinical research regulations (FDA, OHRP), and medical terminology.
Proficiency with Microsoft Office Suite (Word, Excel, Outlook, Access).
Tracking, recordkeeping, and analytical skills for data management.
Strong organizational, writing, and communication abilities.
Ability to work occasional overtime and travel on occasion.
HS or GED equivalent and/have demonstrated skills to perform duties.
Minimum 2 years of experience coordinating clinical trials.
Bachelor’s degree in a related area.
Certification by SoCRA or ACRP preferred.
Previous oncology‑related clinical research experience preferred.
Preferred Qualifications
Experience with cancer‑related protocols and on‑core data management.
Experience coordinating Phase I or maintenance clinical trials.
SoCRA or ACRP certification.
Salary Assistant CRC: $29.02–$46.72 per hour. CRC: $32.01–$51.48 per hour. Hourly, 100% full time, Monday‑Friday 8:00‑17:00.
Location & Shift Sacramento, California – Facilities Support Services Building (HSP068). Hybrid – mix of on‑site and remote work.
Benefits Full range of UC Davis benefits: medical, dental, vision, paid holidays, sick leave, PTO, pregnancy & parental leave, retirement, and professional development grants. Union representation: RX‑Research Professionals.
EEO Statement 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.
Application Deadline Apply by 10/25/2025 at 11:59pm.
Important This position is not a H‑1B visa opportunity and does not require a H‑1B visa application.
Contact To apply or learn more, visit the UC Davis Comprehensive Cancer Center job portal or contact your recruiter.
#J-18808-Ljbffr