Job Description
Job Description
Clinical Research Coordinator 1449575
- Hourly pay : $45 / hr
- Worksite : Leading university (Palo Alto, CA 94304 - Onsite)
- W2 Employment, Group Medical, Dental, Vision, Life, Retirement Savings Program, PSL
- 40 hours / week, 5 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 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 :
2+ years of clinical research experience in an academic setting.Shift :
Monday to Friday from 8 am to 5 pm.