RN Research Nurse Coordinator I - Center for Clinical Studies job opportunity at WashU.

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WashU RN Research Nurse Coordinator I - Center for Clinical Studies
Experience: 2-years
Pattern: full-time
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Research nurse

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degreeBachelor's (B.Sc.)
loacation On Campus/Onsite locations Washington University Medical Campus, United States Of America
loacation On Campus/Onsi..........United States Of America

Job Description Primary Duties & Responsibilities: Works under the principal investigator’s guidance to meet the research objectives of the project. Provides direct patient care, including assessment, planning, implementation and evaluation of patients; documents, collects #data and #assists #physicians. Works with staff to identify, screen and enroll study subjects; ensures lab and data are obtained according to established protocol. Prepares/submits event reports in adherence with study procedures, budget and established guidelines. Assists research associates from sponsoring organization, providing study explanations and reports as necessary. Collects basic health information as required by protocol. Performs clinical study visits and schedules patients for exams and tests in accordance with study protocol. Performs vital signs, blood draws, various tests and minor procedures according to protocol and within direction of PI and personal skill set. Helps implement and independently performs research study and clinical procedures including assessment, planning, implementation, and evaluation of participants to generate study data according to established protocol; collects data (e.g., basic health information and vital signs), may perform blood draws and minor procedures according to protocol and within the direction of PI and personal skill set; documents processes as required by protocol; monitors and manages participants in the Clinical Translational Research Unit; assists principal investigators and physicians. Serves as the contact person for research participants; provides study participants, families, and caregivers education about the studies, dementia, and dementia care. Coordinates handling of specimens, administration of clinical trials, collection of source information, case reporting, and participant payments. Designs, implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; identifies problems and/or inconsistencies and monitors participant’s progress to include documentation and reporting of adverse events; resolves IRB/protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency.

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