Clinical Research Coordinator

$25/hr - $35/hr (depending on experience) Monday-Friday, On Site Schedule Responsibilities Patient recruitment and enrollment Obtaining informed consent per ICH/GCP and site SOPs Reviewing and revising source documents and interviewing and collecting data from study participants Participating in protocol training meetings and completing online training for protocol-specific software programs Dispensing/collecting study medication and providing accurate Investigational Product accountability Working with our lab specialist to obtain study participant laboratory specimens according to protocol Completing study participant tracking information (either electronic or manual) accurately and on a timely basis. Responding and resolving data queries in a prompt manner Maintaining a thorough understanding of all data collection instruments and collecting data accurately and according to protocol Performing basic data manipulation Maintaining a thorough understanding of all assigned clinical trial protocols Other duties as assigned Qualifications 1+ years of experience as a CRC with a research site Bachelor's degree preferred Phlebotomy and EKG experience preferred (Not Required) Familiar with e-source reporting via an electronic platform #J-18808-Ljbffr