Job Description

• 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 technology company seeks a Clinical Research Coordinator to join the clinical trials officeThe 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!

• 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.

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