Clinical Research Coordinator (Hybrid) - Medical Oncology job opportunity at WashU.

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WashU Clinical Research Coordinator (Hybrid) - Medical Oncology
Experience: 1-year
Pattern: hybrid
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Research coordinator

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degreeBachelor's (B.Sc.)
loacation Hybrid locations Washington University Medical Campus, United States Of America
loacation Hybrid locatio..........United States Of America

Job Description Primary Duties & Responsibilities: #Manages patient-related #data across all phases of clinical trials; ensures compliance with protocol guidelines and requirements of regulatory agencies; identifies procedural problems and/or inconsistencies. Monitors participant’s progress throughout study, which includes documentation and reporting of adverse events; resolves protocol #management issues and recommends corrective action as appropriate; serves as liaison between WU study team, the sponsor, and Clinical Research Organization (CRO). Extracts clinical data from EMR and receives clinical data from other source documents and enters it in a study specific electronic data capture system (EDC). Assures protocol compliance and adherence by performance of quality control checks of collected data. Evaluates all lab and clinical assessments to ensure they are completed correctly and per protocol specification. Reviews collected clinical data in conjunction with PI or sub-investigator as appropriate. Frequently communicates with sponsors and CROs, and responds to queries. Facilitates sponsor monitoring visits (if applicable). Attends patient-related, protocol, and educational meetings. May prepare oral or written presentations related to patient updates or protocol training. Attends sponsor monitoring meetings with the PI (if applicable). Performs other duties incidental to the work described herein. Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants’ progress in the study; analyzes, investigates and reports adverse events; makes decisions as to when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants; resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency. Recruits and enrolls study participants; makes and/or participates in making determinations of eligibility based on diagnostic criteria and/or observations/analysis in participant interviews; develops informed consent packets for study participants and confers with participants to explain purpose of study and obtain completed informed consent packets; explains diagnostic procedures and treatment plans to address participant/family concerns; administers/scores tests and/or evaluates all lab and clinical assessments to ensure they are completed in a timely manner. Ensures timely completion of all protocol requirements (assessment, lab testing, procedures and treatments), to include scheduling and facilitating the patient’s timely completion of protocol requirements; evaluates and interprets collected clinical data as appropriate; prepares oral or written presentations or reports and analyses setting forth progress trends and provides recommendations or conclusions of the same. Collects clinical data under clinical research protocols. Performs other duties as assigned.

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