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Job #03329

About our client Our client is a well-established CRO. They have an experienced management team and a loyal customer base. They have developed an industry-wide reputation for a positive work environment and an aggressive training program that ensures employees are up-to-date on current trends and best practices. This is a strong opportunity for someone that wants to put their drive and initiative to work. Position Location Clinical Research Coordinator Louisiana Salary Highly competitive package, commensurate with experience Responsibilities 1) Assist in recruiting and screening patients, implementing protocols, administering informed consent and completion of CRFs 2) Oversee teams to appropriately designate work duties and continually monitor safety/efficacy as well as project efficiencies 3) Work with teams to analyze and evaluate data 4) Ensure compliance with overall objectives 5) Perform a variety of complicated tasks to ensure safety and efficacy 6) Meet the overall team and company goals 7) Coordinate internal/external clinical laboratory arrangements and initiate appropriate correspondence 8) Provide medical information for evaluation and screening of volunteers for study participation 9) Assist in developing forms and review for each study project (CRFs, sample labels and data collection forms) 10) Develop summary information for each protocol and coordinate protocol review meetings for Clinical staff Requirements 1) BS in a scientific field 2) Minimum 2 years of experience as a Clinical Research Coordinator 3) Experience in clinical trials (Phase II – IV) 4) Familiarity with clinical trial documents 5) Excellent IT (MS Word and spreadsheet) skills