Hybrid Clinicial Research Coordinator 2

Hybrid Clinical Research Coordinator 2
Pay Rate Range: $40.00 - 45.00/hr (W2)
Employment Type: Contract (Potential Temp-to-Hire)
Duration: 07/01/2026 12/31/2026
Schedule: Full-Time Monday Friday (Day Shift)
Hours: 40 hours/week
Work Arrangement: Hybrid
Location: Palo Alto CA (780 or 800 Welch Road)
Job Code:

Tekberry offers a $100 payment for referrals!

Tekberry is seeking an experienced Clinical Research Coordinator 2 to support our client within the School of Medicine. This role independently manages significant aspects of oncology clinical research studies ensuring the successful execution of research protocols while maintaining regulatory compliance and exceptional participant care.

The ideal candidate will have hands-on experience supporting oncology treatment trials particularly Phase I studies within a healthcare institution. Candidates with experience limited to CRO or pharmaceutical CRA environments will not be considered.

• Independently coordinate and manage all aspects of assigned clinical research studies
• Oversee participant recruitment screening enrollment and retention efforts
• Develop strategies to achieve study enrollment goals and maintain participant engagement
• Manage study data collection processes and oversee data integrity
• Develop and maintain systems to organize collect monitor and report research data
• Extract analyze and interpret study data to support research objectives
• Develop project timelines milestones and accountability measures
• Lead study meetings and prepare meeting documentation and minutes
• Collaborate with principal investigators sponsors and study teams
• Monitor and report serious adverse events and resolve sponsor queries
• Ensure ongoing compliance with study protocols HIPAA FDA regulations Good Clinical Practice (GCP) and Institutional Review Board (IRB) requirements
• Prepare and submit IRB applications renewals and modifications
• Conduct audits of study operations and implement corrective actions when necessary
• Assist with study budget development and distinguish standard-of-care versus research-related procedures
• Track study milestones and support sponsor invoicing activities
• Mentor train and provide guidance to junior staff and students as assigned
• Support Investigational New Drug (IND) submissions to the FDA when applicable

• Bachelors degree in a related field
• Minimum of 2 years of clinical research experience or an equivalent combination of education and experience
• Direct experience supporting oncology treatment trials
• Experience supporting Phase I clinical trials
• Experience working onsite within a healthcare institution (hospital academic medical center or clinical setting)
• Experience with EPIC electronic medical records system
• Strong understanding of:
  • HIPAA regulations
  • FDA regulations
  • Institutional Review Board (IRB) processes
  • Good Clinical Practice (GCP) guidelines
• Knowledge of medical terminology
• Strong interpersonal organizational and communication skills
• Proficiency with Microsoft Office and research databases

• Experience supporting Phase II or Phase III oncology trials
• Previous experience in an academic medical center environment
• Experience independently managing multiple research protocols simultaneously
• Experience mentoring junior research staff
• Certification through ACRP or SOCRA preferred

• Hybrid work arrangement with onsite responsibilities at Stanford facilities
• Frequent standing walking bending twisting and participant interaction
• Occasional lifting carrying pushing or pulling up to 40 pounds
• Regular use of computers telephones and electronic research systems
• May involve interaction with patients undergoing active treatment protocols
• Ability to work in a fast-paced clinical research environment while maintaining strict attention to detail and regulatory compliance

We need hard-working reliable employees. If youre ready to contribute to groundbreaking oncology research and support studies that improve patient outcomes we want to hear from you!

Tekberry is an equal opportunity employer. All qualified applicants will receive consideration without regard to race color religion sex sexual orientation gender identity national origin disability or veteran status. Tekberry is a certified Minority Business Enterprise (MBE) and Disadvantaged Business Enterprise (DBE).

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