"Alerted.org

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 technology company 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 Coordinator 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 Coordinator 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.