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WA
RN Research Nurse Coordinator II - Neurology
Washington University in St. LouisMcMillan Hospital, United States, United Statesfull_timeVerifiedPosted 30 Apr 2025
💰 $105,700/yr($60,800/yr – $105,700/yr)
About the role
Scheduled Hours
40Position Summary
Position functions as the lead person on a research project; coordinates enrollment of study subjects; ensures adherence to study procedures consistent with the study protocol and verifiable source documentation; may supervise personnel assigned to work on the study. Coordinates with multidisciplinary teams to maintain continuity of care and human subject protection with a commitment to research integrity. May perform duties inclusive of those delegated to a Research Nurse Coordinator I.Job Description
Primary Duties & Responsibilities:
- Works under the Principal Investigator’s (PI) guidance to meet the research objective of the project.
- Facilitates and implements study start-up activities, including, but not limited to: trial feasibility assessment; study logistics; IRB (both local and central) submissions and other applicable regulatory requirements; budgetary and contract review and approval.
- Provides direct patient care, including assessment, planning, implementation and evaluation of patients; documents, collects data and assists physicians.
- Works with research team to identify, screen and enroll study subjects.
- Ensures protocol requirements are met, including, but not limited to: direct contact with research participants; collection of basic health information; coordination of study related procedures; handling, processing and shipping of research specimens, source documentation and data entry.
- May train and supervise staff assigned to work on the research project(s).
- Coordinates handling of specimens, administration of clinical trials, collection of source information and case reporting.
- Prepares/submits reportable event reports to sponsor(s), IRBs and regulatory agencies in accordance with the study protocol and established policies, procedures, and regulations.
- Collaborates with sponsor’s research associates during monitoring activities by providing study documentation, data clarifications and reports as necessary.
- Authorizes payments to ancillary organizations for services rendered and reconciles payments from organizations serviced.
- Demonstrates experience in clinical trials management including strong organizational skills, independence and resourcefulness and an increased responsibility for the day-to-day conduction and oversight of multiple clinical trials.
- Provides oversight of administration of study medications and/or study interventions, as appropriate. Administers investigational products in approved settings.
- Educates staff nurses caring for research patients by providing necessary information about the research study including intervention and potential adverse events and required study procedures.
- Performs other duties incidental to the work described above.
Working Conditions:
Job Location/Working Conditions
- Normal office environment
- Exposure to blood-borne pathogens
- Requires protective devices
- Patient care setting
- Direct patient care setting
Physical Effort
- Typically sitting at desk or table
- Typically bending, crouching, stooping
- Occasional lifting (25 lbs. or less)
Equipment
- Office equipment
- Clinical/diagnostic equipment
Required Qualifications
Education:
A diploma, certification or degree is not required.
Certifications:
Work Experience:
Skills:
Driver's License:
More About This Job
Required Qualifications:
- Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirements).
Preferred Qualifications:
- Clinical Research C
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