Clinical Research Coordinator I

Responsibilities include but are not limited to being lead coordinator on a study, executing follow-up visits ongoing studies, query resolution and other study specific tasks. The CRC I will perform daily tasks such as document review, data entry, test material preparation and data collection. This position may coordinate and execute projects assigned by the Clinic Manager while abiding by Good Clinical Practice (GCP) guidelines.JOB FUNCTIONSPerforms station and instrumentation duties on other studies as assigned, including the collection and recording of clinical informationResponds to queries from Quality Assurance and Statistics departmentsSets up and conducts study in compliance with protocol, SOPs, applicable regulations and GCPsPrepares for and conducts pre-study meetings as well as other meetings and processes as deemed to protocol, SOPs and GCPsMonitor Compliance of panelistsPrepares and is accountable for all Test Material for managed studiesAdheres to study budgetPrepares, completes, organizes and maintains of all study documentation forms, including drafting protocol amendments, case report forms, Electronic Data Capture (EDC), and other study specific documentsAssures that staff working on their managed studies understand and are performing duties according to protocol, SOPs and GCPsCoordinates scheduling subjects for visitsCompletes other duties or tasks assigned by Clinic Manager and/or SupervisorJOB COMPLEXITYMulti-tasking is keyIMPACT OF DECISIONSMake decisions as a study leaderANALYTICAL THINKING/PROBLEM SOLVING Handle issues with panelists and create solutionsArrange work for studies