Billing, Budget Management, Case Report Form (CRF), Clinical Research, Clinical Trial, Data Management, Documentation, IRB/IEC (Institutional Review Board/Independent Ethics Committee), Maintain Compliance, Medical Terminology, Microsoft Office, Oncology, Operational Support, Organizational Skills, Patient Safety, Problem Solving Skills, Recruiting Strategy, Regulations, Regulatory Compliance, Regulatory Requirements, Research Protocols, Safety Standards, Sample/Specimen Processing, Society of Clinical Research Associates (SoCRA), Specimen Collection, Startup
Clinical Research Coordinator 1492365
- Hourly pay: $44/hr
- Worksite: Leading university (Stanford, CA 94305 - Onsite)
- W2 Employment, Group Medical, Dental, Vision, Life, Retirement Savings Program, PSL
- 40 hours/week, 6 Month Assignment (With possibility of extension)
A leading university is seeking a Clinical Research Coordinator to support oncology clinical trials. This role will coordinate study activities from start-up through closeout, ensuring protocol compliance, patient safety, and accurate data management across Phase I–III treatment studies.
Clinical Research Coordinator Responsibilities:
- Coordinate clinical studies from initiation through closeout, serving as the primary contact for participants, sponsors, and regulatory agencies while ensuring adherence to study protocols and patient safety standards.
- Screen, recruit, and consent study participants; support recruitment strategies; coordinate study visits, specimen collection and processing, and assemble study kits for clinical procedures.
- Collect, manage, and maintain patient and laboratory data, including case report forms, study databases, flow sheets, and essential regulatory documentation in compliance with institutional and regulatory requirements.
- Ensure compliance with protocols and regulatory standards by preparing submissions, maintaining IRB approvals, reviewing data for accuracy, and participating in monitoring visits and audits.
- Support operational and financial aspects of studies, including scheduling procedures, coordinating vendor and sponsor interactions, monitoring study budgets, resolving billing issues, and maintaining communication with principal investigators and stakeholders.
Clinical Research Coordinator Qualifications:
- 1-2 years of clinical research experience, preferably in oncology and Phase I–III treatment trials.
- Bachelor’s degree in a related field, OR,
- 2-year college degree with 2+ years of relevant experience, or equivalent combination of education and experience.
- Strong knowledge of medical terminology and proficiency with Microsoft Office.
- Clinical research certification (SoCRA or ACRP) is preferred.
- Ability to drive day or night if required.
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