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DescriptionJob Opportunity: Clinical Non-Licensed Pool - Clinical Research Coordinator Facility: CSMN - 1102083 - TACRI Research Location: Los Angeles, CA Employment Type: Travel/Contract Shift: Day (5x8 Hours) 8:00 17:00 Start Date: 3/24/2025 Job Duration: 13 weeks Compensation: Rate Type: Hourly Over Time: Default Multiplier: None; 8 Hour Multiplier: 40 total hours in 1 week: 1.3%; 10 Hour Multiplier: 40 total hours in 1 week: 1.3%; 12 Hour Multiplier: 48 total hours in 1 week: 1.3%; Double Time: 12 total hours in a day: 1.7% On-Call: 8$ Call Back: 1% Holiday Pay: 1.5% Additional Information: Required: * Associates Degree * 3 years of Clinical Research Experience * BLS Preferred: * Bachelors Degree * SoCRA or ACRP Certification * Phlebotomy Certified * Medical Assistant Diploma * Experience with Oncology setting Primary Duties and Responsibilities * Establishes and executes logistical aspects of clinical research projects to achieve project objectives, including project planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety. * Coordinates administrative functions of research studies, including scheduling of patients for research visits, procedures and labs and completion and maintenance of consent forms, case report forms, SAE's and source documents. * Responsible for screening and recruitment of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and supporting the informed consent process. * Responsible for accurate and timely data collection, documentation, entry and reporting, including resolution of queries from sponsors or regulatory entities. * Coordinates institutional, pharmaceutical and internal audits, including facilitating third party study monitoring and designs and implements needed corrective actions. * Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings. * Responsible for timely submission of adverse events, serious adverse events, protocol deviations, and Safety Letters in accordance with local and federal guidelines. * Identifies quality and performance improvement opportunities and collaborates with staff in the development of action plans to improve quality. * Plans and coordinates strategies for increasing research participant enrollment, and/or improving clinical research efficiency as needed. * Provides technical support for the preparation of grant proposals, publications, presentations and special projects. * Provides assistance with research project budget development, including identifying and classifying routine care vs. research related care and provides assistance with research participant research billing and reconciliation. * Attend meetings and conferences related to research activities, including research staff meetings. * Participate in planning, workshops, evaluation meetings, and seminars, educational or administrative meetings as necessary or requested; Participates in training and education of new research personnel.