Clinical Research Coordinator Associate The Division of Quality of Life and Pediatric Palliative Care is seeking a Clinical Research Coordinator Associate to conduct clinical research on progressively more complex projects and assignments. Independently manages significant and key aspects of large studies or all aspects of one or more small research studies. This is an onsite role requiring you to be on campus in Palo Alto, CA. The Division is a growing team. The Division activities reaches all parts of the mission: patient care, education, and research. The Clinical Research Associate will have a great deal of exposure to all these areas and will communicate with a broad range of individuals at the Executive level, internally and externally. Within the Division, there is a strong operations team of about 20 people. We are a supportive group that prioritizes well-being, with many team events and opportunities for professional development and personal growth. We value balancing home and work life. We foster an environment that leads to fulfilling and rewarding careers at Stanford University for all staff. Please check out our website and social media channels below and come see about working for an organization that directly impacts the lives of children. Duties include: Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies. Coordinate collection of study specimens and processing. 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. Conduct qualitative analyses of interview, focus group and other data. 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. Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct. Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements. Participate in monitor visits and regulatory audits.
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