Clinical Research Coordinator CRC

Clinical Research Coordinator (Rancho Cucamonga)

Part time Position for Clinical Research Coordinator in a busy Rancho Cucamonga office.
This individual must have working knowledge of Clinical trials, State, Federal and Local Regulations, IRB requirements, consent form and protocol.
Well versed in Good Clinical Practices, Food and Drug Administration Rules and Regulations and HIPAA regulations in relation to clinical trials. This position requires the individual to be able to multitask and have experience from startup to close out and should have excellent written and verbal skills. A Clinical Research Coordinator is responsible for a variety of duties including:

• Assist with all clinical research activities with moderate supervision with the ability to multi-task.and demonstrate excellent organizational skills
• Screen, recruit and enroll patients/research participants with the ability to communicate egffectively both orally and in writing
• Participate in the informed consent process of study subjects while supportingthe safety of clinical research patients/research participants
• Comply with institutional policies, standard operating procedures (SOPs) and guidelines, understand good clinical practice (GCP) and regulatory compliance and Adhere to IRB approved protocols
• Maintain study source document
• Managing budgets set aside for research
• Coordinate protocol related research procedures, study visits, and follow-up care
• Report adverse events, Monitor studies to verifiy that the rights and well-being of human subjects are protected, the reported trial data are accurate, complete and verifiable from source documents and the conduct of the trial is in compliance with the currently approved protocol/amendment(s), with GCP (Good Clinical Practice) and with the applicable regulatory requirements
• Maintaining research records of study activity in accordance with the guidelines set by the FDA (Food and Drug Administration and follow Good Clinical Practice (GCP)
• Assisitng with the collection, labeling, storage and transport of all specimens
• Making sure that all equipment and supplies needed for the study are in-stock and in good working order

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