Clinical Research Coordinator
$83,200–$104,000 year
Hybrid · Stanford, California, United States
Job Summary
Clinical Research Coordinator will independently manage oncology clinical research activities at a leading university in a hybrid Stanford, CA setting. Responsibilities include subject recruitment, enrollment and retention, data management, coordinating study operations, supervising research staff or students, supporting budgets and sponsor invoicing, ensuring regulatory compliance (IRB submissions, FDA/IND activities, HIPAA, GCP), monitoring adverse events, and collaborating with investigators and sponsors to optimize protocol execution and processes. Required qualifications include a Bachelor's degree, 2+ years in clinical research, oncology trial coordination, Phase I experience, EPIC proficiency, onsite healthcare experience, regulatory knowledge, medical terminology, MS Office/database skills, and a valid driver’s license.
Required Qualifications
- Bachelor's degree in a related field
- 2+ years of clinical research experience or equivalent
- Experience coordinating oncology treatment trials
- Experience supporting Phase I clinical trials
- Experience using EPIC electronic medical record systems
- Onsite work in healthcare institution
- Knowledge of HIPAA, FDA regulations, IRB requirements, and Good Clinical Practice
- Knowledge of medical terminology
- Proficiency with Microsoft Office and database systems
- Valid driver's license
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