- Shift : Day 5x8-Hour (08 : 00 - 17 : 00) -Work location : Onsite; Los Angeles, CA-Compensation : $40 to $44 per hourDuties 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 protocolcompliance 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 sourcedocuments.
- Responsible for screening and recruitment of potential patients for protocol eligibility, presenting non-medicaltrial concepts and details to the patients and supporting the informed consent process.
- Responsible for accurate and timely data collection, documentation, entry and reporting, including resolutionof queries from sponsors or regulatory entities.
- Coordinates institutional, pharmaceutical and internal audits, including facilitating third party studymonitoring 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 staffmeetings.-Responsible for timely submission of adverse events, serious adverse events, protocol deviations, and SafetyLetters in accordance with local and federal guidelines.
- Identifies quality and performance improvement opportunities and collaborates with staff in the developmentof action plans to improve quality.
- Plans and coordinates strategies for increasing research participant enrollment, and / or improving clinicalresearch efficiency as needed.
- Provides technical support for the preparation of grant proposals, publications, presentations and specialprojects.-Provides assistance with research project budget development, including identifying and classifying routinecare vs.
research related care and provides assistance with research participant research billing andreconciliation. Education Qualifications-Bachelor's Degree (BSN)Experience-1 year of clinic research experience-Cardiology experience-Vascular experience-Epic / CS Link experienceLicenses and Certifications -Certified Clinical Research Coordinator (CCRC)Benefits-Health / Dental / Vision Insurance-Sick time off
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