Job Title:
Assistant Clinical Research Coordinator / Clinical Research Coordinator
Employer:
University of California - Davis Health
Location:
United States, California, Sacramento
Job ID:
77423
Start Date (Posted):
08 April 2025
Apply By Date:
18 April 2025, 11:59 PM (PST)
Job Type:
Full-Time, On-Site
Salary Range:
Assistant CRC: $29.02 – $46.72 per hour
CRC: $32.01 – $51.48 per hour
Work Schedule:
Monday – Friday, 8 AM – 5 PM
Benefits:
Vision and dental insurance (premiums covered for employees and family)
Parental leave, pregnancy & family medical leave
Paid holidays, vacation, and sick time
Tuition reimbursement & CE allowance
Long-term disability & supplemental insurance options
Retirement benefit options (Pension and Savings Plans)
Free professional development & wellness programs
Public Service Loan Forgiveness qualified employer
Department:
UC Davis Comprehensive Cancer Center (UCDCCC) – Office of Clinical Research (OCR)
Focus: Coordination of cancer-related clinical research trials from development through compliance and reporting
Key Responsibilities:
Assistant CRC:
Study Management (50%)
Data Management (30%)
Quality Assurance (15%)
Other duties (5%)
CRC:
Study Management (80%)
Quality Assurance (15%)
Other duties (5%)
Both roles include:
Supporting all aspects of cancer trial operations
Assisting with patient recruitment, screening, and consenting
Coordinating communication with sponsors and regulatory bodies
Maintaining records and entering trial data into OnCore
Attending Disease Team Committee (DTC) meetings
Ensuring adherence to IRB, FDA, and NCI reporting guidelines
Minimum Qualifications:
Assistant CRC:
Minimum 1 year of relevant experience
Knowledge of clinical research regulations (FDA, OHRP)
Understanding of medical terminology, anatomy, and disease processes
Proficiency in Microsoft Office Suite
Strong organizational, analytical, and writing skills
Willingness to travel occasionally and work overtime
CRC (In addition to above):
Minimum 2 years of experience coordinating clinical trials
Advanced knowledge of clinical trial regulations and data management
Demonstrated critical thinking and good judgment
Preferred Qualifications:
Certification from SoCRA or ACRP
Bachelor's degree in a related field
Previous oncology research experience
Physical & Environmental Demands:
Frequent standing, walking, lifting (up to 50+ lbs), and operating vehicles/equipment
Exposure to chemicals, radiation, temperature changes
Sustained mental concentration, multitasking, and patient contact
Work Environment:
100% on-site at the Cancer Center
UC Davis is a smoke and tobacco-free campus
Occasionally requires overtime and travel
Special Requirements:
Background check, drug screening, and medical evaluation
Mandated reporter under CANRA
Disclosure of past misconduct as per UC policies
Diversity & Inclusion Statement:
UC Davis fosters a culture of belonging, inclusivity, and equal opportunity. Applicants from all backgrounds are encouraged to apply. The university values diverse perspectives and strives to create a vibrant and equitable workplace.
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