Cancer Clinical Research Coordinator Associate

Duration: 06 months (Possibilities of extension)Shift: 1st Shift (8-5, Monday through Friday) Hiring Manager Note:**Oncology exp is a must. Scheduling app, data enter, Coordination** Job Description:·       The Clinical Trials Office in the Stanford Cancer Institute, in Stanford University’s 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.·       Stanford 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:·       How many years of experience are required? 1 - 2·       Top 3 requirements to hire? Coordinator site experience (not pharma, CRO, or Lab research experience), treatment trials experience, EPIC experience, and a like to have is oncology experience.Company DescriptionSelect Source International (SSI) is a distinguished staffing company with nearly 25 years of experience, renowned for delivering top-tier workforce solutions encompassing staffing, recruiting, and managed services. As a proud supplier, we bring a wealth of expertise and best-in-business differentiators to comprehensively support your diverse workforce needs.Based in Minneapolis, Minnesota, USA, SSI has established itself as a global leader, serving a broad clientele across industries with unwavering dedication and excellence. SSI is ISO 9001, 14001, and Soc2 Type2 certified, underscoring our commitment to quality and security. We have garnered numerous sustainability and supplier diversity awards, further validating our industry-leading capabilities

Salary : $33 - $36