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Washington University in St. Louis

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St. Louis, Missouri, USA

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"RN Research Nurse Coordinator II - Cardiology"

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RN Research Nurse Coordinator II - Cardiology

Position Summary

This highly organized and data-focused RN supports cardiology clinical trials through coordinating and implementing research studies, enrolling eligible patients and ensuring thorough documentation of data collection. Our Cardiology clinical trials help us to understand further and treat diseases and conditions of the heart and vascular system as well as assist in the development of treatments and strategies to maintain heart health and improve patient outcomes.

Our physicians and research staff collaborate to bring the most current and cutting-edge research studies to our patients. This position offers the opportunity to work on diverse study types, including drug efficacy, device evaluations, procedural comparisons and registry studies. Our team works collaboratively with many healthcare professionals to support a variety of research protocols.

The ideal candidate would be an RN with current or recent analytical research experience. A cardiology Nursing experience background would be a plus!, with the ability to communicate effectively and interact professionally with patients, families and research staff.

This is a M-F day position on-site at the BJH/Wash U Medical Center location on Kingshighway, across the street from Forest Park.

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: Basic Life Support - American Heart Association, Basic Life Support - American Red Cross, Registered Nurse - Illinois Department of Financial and Professional Regulation, Registered Nurse - Missouri Division of Professional Registration. Work Experience: Related Nursing Or Research (2 Years).

Preferred Qualifications

Education: B.S. - Bachelor of Science - Nursing, B.S.N. - Bachelor of Science in Nursing. Work Experience: Academic Research Setting (2 Years). Skills: Active Listening, Clinical Research Coordination, Clinical Research Management, Clinical Research Methods, Clinical Research Operations, Clinical Techniques, Database Management, Detail-Oriented, Effective Written Communication, Electronic Health Records (EHR), Nursing Fundamentals, Oral Communications, Patient Recruitment, Reporting Tools, Spreadsheet Software, Statistical Analysis Software (SAS), Team Collaboration.

Grade

S26

Salary Range

$60,800.00 - $105,700.00 / Annually

10

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