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Clinical Research Coordinator
Clinical Research CoordinatorAvispa Technology • Palo Alto, CA, US
Clinical Research Coordinator

Clinical Research Coordinator

Avispa Technology • Palo Alto, CA, US
[job_card.30_days_ago]
[job_preview.job_type]
  • [job_card.full_time]
[job_card.job_description]

Job Description

Job Description

Clinical Research Coordinator 1458001

  • Hourly pay : $35 / hr
  • Worksite : Leading university (Palo Alto, CA 94304 - Onsite)
  • W2 Employment, Group Medical, Dental, Vision, Life, Retirement Savings Program, PSL
  • 40 hours / week, 5-6 Month Assignment, Possible extension / conversion

A leading university seeks a Clinical Research Coordinator to join the clinical trials office . The successful candidate will work with the team to ensure the safety and well-being of trial participants and to document related data per protocols and internal guidelines. The company offers a family-oriented culture and environment!

Clinical Research Co ordinator Responsibilities :

  • Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out.
  • Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies.
  • Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets and other study related documents, and complete study documents / case report forms.
  • Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. Prepare regulatory submissions, and ensure Institutional Review Board renewals are completed.
  • Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.
  • Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and / or management staff.

    • Clinical Research Coordinat or Qualifications :

  • 1-2 years of related experience.
  • Coordinator site experience (not pharma, CRO, or Lab research experience).
  • Treatment trials experience.
  • EPIC experience.
  • Oncology experience.

    • Shift :

  • Monday to Friday from 8 am to 5 pm.

    • (H)

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    Clinical Research Coordinator • Palo Alto, CA, US

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