Full Time Clinical Research Coordinator - (Amarillo, TX)

Full-time Clinical Research Coordinator Duties To Include But Are Not Limited To: " Under the direct supervision of the study team, assists in the coordination of the info of the human research subject study and documentation concerning study protocols. " Must possess knowledge of IRB and human subject protection and must adhere to an IRB approved protocol. " Coordinate all clinical research activities with moderate supervision. " Understand good clinical practice (GCP) and regulatory compliance. " Collect, process and ship laboratory specimens. " Requires effective writing and communication, work as part of a team, expertise to multitask. Min Requirements: " Associates or Allied Health Degree " 1 yr Clinical Research Background " Certified Clinical Research Coordinator Is an Added Plus Strong Comp plan Includes: Excellent Salary Paid Vacation, Holidays, and Sick Time Profit Sharing Retirement package Health Insurance Lubbock Avalanche-Journal.Category: Science, Keywords: Clinical Research Coordinator