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Salary
$68k per year
Location
Hybrid (Palo Alto, United States)
Seniority
Junior · 1+ year exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 29, 2026. First seen by Alion on Oct 28, 2026. Avispa scores A on the Alion truth index.

Overview
Company
Impact
Profile match
Avispa is a US workforce solutions firm based in Truckee, California, providing staff augmentation, contract-to-hire and direct-hire recruiting, statement-of-work management, employer-of-record and agent-of-record services, and managed service provider programs. The MBE-certified company places W2 contractors at corporate clients such as universities, health systems, streaming networks and manufacturers, runs supplier management on clients' vendor management systems, and offers employer-of-record coverage in five jurisdictions. It recruits contract staff for finance, payroll, operations, clinical research, Epic and healthcare IT, marketing operations and manufacturing roles.

Assistant Clinical Research Coordinator 1503779

  • Hourly pay: $34/hr
  • Worksite: Leading university (Palo Alto, CA 94304 - Hybrid)
  • 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 an Assistant Clinical Research Coordinator to support the coordination and execution of clinical research studies. This role assists with participant recruitment, data collection, regulatory documentation, and study operations while ensuring compliance with research protocols and regulatory requirements.

Assistant Clinical Research Coordinator Responsibilities:

  • Coordinate study activities by scheduling participant visits, assisting with recruitment, screening, informed consent, follow-up communications, and processing study compensation upon completion.
  • Collect, review, and maintain accurate clinical research data by administering study questionnaires, extracting information from medical records, completing case report forms, and ensuring data quality and completeness.
  • Prepare and maintain regulatory and study documentation, including consent forms, subject logs, correspondence, and other research records in compliance with study protocols and regulatory requirements.
  • Support clinical research procedures by collecting and processing study specimens, performing basic patient measurements and tests (such as vital signs, phlebotomy, and EKG after appropriate training/certification), and preparing specimens for shipment.
  • Maintain study operations by ordering supplies, managing research equipment, collaborating with the study team, and supporting additional study activities as assigned.

Assistant Clinical Research Coordinator Qualifications:

  • 1 year of clinical research or related experience.
  • Experience with clinical research data entry and electronic medical records (EPIC is preferred).
  • General knowledge of medical terminology.
  • Ability to maintain accurate research documentation and regulatory records with strong organizational, communication, and attention-to-detail skills.
  • Working toward certification to perform basic patient procedures, such as phlebotomy and EKG, is preferred.
  • Valid California Class C Driver's License.

Shift:

  • Hybrid: 3-4 days onsite per week.
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