Clinical Research Assistant

Duties And Responsibilities (Responsibilities Necessary To Accomplish Job Functions) Assists coordinators with patient visits including scheduling/tracking, data acquisition/data entry, procedures such as biopsies, administration of photodynamic therapy, adhesive lesional stripping, and related tasks.Assists with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocolAssists physicians with patient care and treatment assisting with instruments, injections, and suture removalCollects EKGs and vital signs Assists clinical trials coordinator and principal investigator with initiation and maintenance of study protocolsAssists with study visits per study protocol, inclusive of source document and case report form completion and submissionPerforms laboratory duties and functions related to study protocols.Ensured clinical trial files are documented in accordance with company standard operating procedures, study protocol and Good Clinical Practice.Reviews exclusion/inclusion criteria with the Principal Investigator or Lead Coordinator to ensure subject eligibilityProcess blood, urine, and biopsy samples in accordance with study protocols and IATA/ OSHA standardsStocks and organizes medical supplies in exam rooms as needed. Notify appropriate personnel when supplies are needed Screen potential research participants and clinical patients for enrollmentWorking knowledge, at minimum, of all applicable protocols. Some team members may be assigned as the primary coordinator for a specific protocol, and should therefore have in-depth knowledge of that protocol Adheres to all safety policies and procedures in performing job duties and responsibilities while supporting a culture of high quality and great customer service.Performs other duties that may be necessary or in the best interest of the organization.