Hybrid Clinical Research Coordinator - Assistant

Avispa Technology

Palo Alto (CA)

Hybride

USD 60 000 - 81 000

Plein temps

Il y a 12 jours

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Avantages offerts par ce poste

Group Medical
Dental
Vision
Life Insurance
Retirement Savings Program
PSL

Résumé du poste

JobScore, Inc. is assisting a leading university in Palo Alto, CA with an Assistant Clinical Research Coordinator.

The role supports coordination and execution of clinical studies, including participant recruitment, data collection, regulatory documentation, and study operations to ensure compliance with protocols. Responsibilities include scheduling visits, screening, consent, data collection, and maintaining accurate records.

Qualifications

  • 1 year or equivalent clinical research experience.
  • Experience with clinical research data entry and electronic medical records (EPIC preferred).
  • General knowledge of medical terminology.
  • Ability to maintain accurate research documentation and regulatory records with strong organization and communication.

Responsabilités

  • Coordinate study activities by scheduling participant visits and assisting with recruitment, consent, follow-up, and compensation.
  • Collect, review, and maintain clinical research data and ensure data quality and completeness.
  • Prepare and maintain regulatory and study documentation in compliance with protocols and regulations.
  • Support procedures by collecting specimens, performing basic measurements (vital signs, phlebotomy, EKG after training).
  • Maintain study operations by ordering supplies and coordinating with the study team.

Connaissances

Clinical research
Data entry
EPIC EMR
Regulatory documentation
Attention to detail

Outils

EPIC

Description du poste

JobScore, Inc. is assisting a leading university in Palo Alto, CA with an Assistant Clinical Research Coordinator.

The role supports coordination and execution of clinical studies, including participant recruitment, data collection, regulatory documentation, and study operations to ensure compliance with protocols. Responsibilities include scheduling visits, screening, consent, data collection, and maintaining accurate records.

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