Client: Educational Provider

Job Title: Clinical Research Coordinator

Location: Palo Alto, CA 94304 - Hybrid Role

Duration: 06 Months (Extension/Conversion based on performance)

Pay Range: ($45-$50) hourly

Summary:

• We are seeking a Clinical Research Coordinator Associate with oncology clinical research experience to support Phase I–III treatment trials in a fast-paced academic research environment.
• This role is responsible for independently coordinating key aspects of clinical studies, including patient recruitment, study operations, regulatory compliance, data management, and sponsor collaboration.

 Responsibilities:

• Coordinate and manage Phase I–III oncology clinical trials from enrollment through closeout
• Support patient recruitment, informed consent, retention, and study visit coordination
• Maintain study documentation, regulatory binders, IRB submissions, and audit readiness
• Manage clinical trial data, EDC systems, query resolution, and compliance tracking
• Monitor AE/SAE reporting and ensure adherence to ICH-GCP, FDA, HIPAA, and protocol requirements
• Collaborate with investigators, sponsors, CRAs, pharmacy, and laboratory teams
• Support monitoring visits, study milestones, and operational process improvements

 Qualifications:

• Bachelor’s degree in a related field
• 2+ years of clinical research coordination experience
• Strong oncology clinical trial experience required
• Experience supporting Phase I–III treatment studies required
• Knowledge of FDA, IRB, HIPAA, and GCP regulations
• Experience with EDC systems and MS Office preferred
• ACRP or SOCRA certification is a plus.

Benefits: