Clinical Research Coordinator
Clinical Research Coordinator 1472429
- Hourly pay: $40-$50/hr
- Worksite: Leading university (Palo Alto, CA 94304 - Hybrid, Must be onsite 4 days per week during training)
- W2 Employment, Group Medical, Dental, Vision, Life, Retirement Savings Program, PSL
- 40 hours/week, 6 Month Assignment
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.
- A bachelor's degree.
- Coordinator site experience.
- Treatment trials and oncology experience.
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