Clinical Research Coordinator

Avispa Technology•Stanford, CA

1d•$44•Onsite

About The Position

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.

Requirements

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.
Ability to drive day or night if required.

Nice To Haves

Clinical research certification (SoCRA or ACRP) is preferred.

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.