Overview

This position supports ORIEN Total Cancer Care research study that is being conducted by the Marker Cancer Center Precision Medicine Initiative. The primary responsibilities for this position include: 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; monitor safety and general well-being of all patients by exercising independent clinical judgment regarding patient care issues and protocol adherence; 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); collaborate and consult with other health professional in planning care for study participation and to ensure protocol compliance; and other duties as assigned.

Source: