Lexington, KY, USA
The primary responsibilities for this position include: obtain, abstract and collate data, reports, etc. related to studies; maintain and submit all reports, forms and updated records to groups required by study; assist in designing a system for organizing, planning and controlling workflow related to the conduct of clinical studies and protocols; coordinate flow of patient through clinical study or protocol, monitoring all events related to patient and communicating any pertinent information to PI and appropriate health professionals; learn basics of Good Clinical Practice (GCP) and standard operating procedures (SOP); monitor safety and general well-being of all patients by exercising independent clinical judgment regarding patient care issues and protocol adherence; assist investigators with identification and recruitment of patients; ensure that per-study and eligibility requirements of the protocol have been met for patients, maintain cooperative and professional relationships with all Clinical Research participants; collaborate and consult with other health professional in planning care for study participation and to ensure protocol compliance; and other duties as assigned.
Interested candidates must complete the application and supply three professional references, as well as, upload a resume, cover letter and as Specific Request 1-copy of your national certification. If the information on your resume is not entered on the application, it will prevent us from being able to assess your education and experience when trying to determine a salary offer.