Clinical Research Coordinator

Cancer Clinical Research Coordinator Associate
The Clinical Trials Office in the Cancer Institute, in School of Medicine seeks a Clinical Research Associate to perform duties related to the coordination of clinical studies.
The incumbent will work with the team to ensure the safety and well-being of trial participants and to document related data per protocols and SCI-CTO SOPS and guidelines.
School of Medicine strives to lead the biomedical revolution by fueling discovery and innovation to advance human health.

Core duties include:
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.
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.
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.

Requirements:
Please attach full job description- attached
Title: Clinical Research Coordinator Associate
Location Address: 800 Welch Road, Palo Alto
Remote/onsite/hybrid: Hybrid and onsite 4 days per week during training
Duration of project (start and end date): approximately 6 months
Full time or part time: Full time
Number of hours per week: 40
Shift timing/schedule: Day
Will the resource be working with minors No
How many years of experience are required 1-2
Will this role extend or possibly convert to a FTE Not initially, however can change
Top 3 requirements to hire Onsite coordinator experience, treatment trials, oncology
Questions that determine what background check package to run
Is a degree required for this job (this will alert that an education check is needed) Yes
Is driving required for this job (this will alert that a MVR is needed) No