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Clinical Research Coordinator

Avispa Technology

Stanford, CA

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JOB DETAILS
SALARY
$51–$51 Per Hour
SKILLS
Adverse Events, Analysis Skills, Auditing, Best Practices, Billing, Budget Management, Calendar Management, Clinical Research, Clinical Trial, Communication Skills, Cross-Functional, Data Analysis, Data Collection, Data Management, Data Quality, FDA (Food and Drug Administration), IRB/IEC (Institutional Review Board/Independent Ethics Committee), Investigational New Drug (IND), Leadership, Maintain Compliance, Mentoring, Microsoft Office, Oncology, Operations Management, Organizational Skills, Performance Analysis, Performance Reviews, Process Improvement, Project Planning, Recruiting Strategy, Regulatory Compliance, Regulatory Requirements, Research Protocols, Retention Programs, Schedule Development
LOCATION
Stanford, CA
POSTED
2 days ago

Clinical Research Coordinator 1492368

  • Hourly pay: $51/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 independently manage key aspects of oncology clinical trials. This role will oversee study operations, data management, and regulatory compliance while driving recruitment strategies and supporting Phase I–III treatment studies.

Clinical Research Coordinator Responsibilities:

  • Independently manage clinical studies or key components of larger trials, including subject recruitment, enrollment strategies, and retention efforts for oncology Phase I–III studies.
  • Oversee data management activities, including developing systems for data collection, analysis, and reporting, and ensuring accuracy and integrity of study data.
  • Lead study operations by developing project plans, schedules, and milestones; facilitating team meetings; and collaborating with principal investigators, sponsors, and cross-functional teams.
  • Ensure regulatory compliance by overseeing IRB submissions, audit readiness, adverse event reporting, and adherence to FDA and study protocol requirements, including IND applications when applicable.
  • Provide leadership and operational oversight by mentoring staff, supporting hiring and performance evaluations, auditing study processes, managing study budgets and invoicing, and driving process improvements and best practices.

Clinical Research Coordinator Qualifications:

  • 2+ years of clinical research experience, preferably in oncology and Phase I–III treatment trials.
  • Bachelor’s degree in a related field, or equivalent combination of education and experience.
  • Strong knowledge of clinical trial operations, data management, and regulatory compliance requirements.
  • Proficiency in Microsoft Office and strong analytical, organizational, and communication skills.
  • Experience working independently with leadership responsibilities in clinical research environments is preferred.
  • Ability to drive day or night, if required.

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About the Company

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Avispa Technology

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