Clinical Research Coordinator, RN

Overview

Join to apply for the Clinical Research Coordinator, RN role at The START Center for Cancer Research.

The START Center for Cancer Research ("START") is the world’s largest early phase site network, fully dedicated to oncology clinical research. START conducts trials to accelerate the development of new anticancer drugs, with research facilities in the United States and in Spain, Portugal, and Ireland. START represents the world’s largest roster of Principal Investigators (PIs) across its eight clinical trial sites and is committed to accelerating passage from trials to treatments to improve patients’ lives.

We are hiring a Clinical Research Coordinator, RN for our Los Angeles, CA location. The Clinical Research Coordinator, RN supports early phase oncology trials under senior research staff guidance, ensuring accurate, timely research conduct, adherence to protocols, regulatory standards, and patient safety. Responsibilities include direct patient interaction, data collection, maintaining Good Clinical Practice (GCP), overseeing multiple protocols, and coordinating patient participation.

The hourly range for this position is between $45.00/hour - $50.00/hour.

• Communicate regularly with Study Sponsors, CROs, and staff regarding protocol status, questions, and concerns.
• Monitor day-to-day study conduct to ensure protocol, SOP, and Good Clinical Practice compliance.
• Review and create trial forms to ensure protocol compliance.
• Maintain organized study files with standardized labeling and filing procedures.
• Implement protocols and amendments, training staff on patient treatment and management.
• Assist with patient screening, eligibility determination, and informed consent process.
• Manage source documents, address protocol deviations, assist with case report forms, and submit Serious Adverse Event reports.

• Associate’s degree in Nursing and RN license in state of California.
• 2 years of clinical research experience, with a basic understanding of oncology Phase 1 trials.
• Strong attention to detail, accuracy in data collection, and ability to meet deadlines.
• Excellent organizational, time-management, and communication skills.
• Proficient in Microsoft Office Suite, clinical trial management software, and knowledge of GCP and regulatory requirements.

• Bachelor’s degree in Nursing.
• Experience working in an oncology setting.

• Comprehensive health coverage:
  Medical, dental, and vision insurance provided
• Robust retirement planning: 401(k) plan available with employer matching
• Financial security:
  Life and disability insurance for added protection
• Flexible financial options:
  Health savings and flexible spending accounts offered
• Well-being and work-life balance:
  Paid time off, flexible schedule, and remote work choices provided
• Collaborative, creative environment that encourages contribution to processes, decisions, planning, and culture

The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted numerous early-phase trials, including therapies approved by the FDA. Learn more at

Join us in our mission to conquer cancer, one clinical trial at a time. Please submit your application online.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.

• Entry level

• Full-time

• Research, Analyst, and Information Technology