RN Research Nurse Coordinator I (PRN) - Cardiology

Washington University in St. Louis•Ann Arbor, MI

1d•$27 - $46•Onsite

About The Position

Position performs duties associated with the coordination and implementation of research study/projects, data collection, and the management of data generated by study protocols. Coordinates with multidisciplinary teams to maintain continuity of care and human subject protection with a commitment to research integrity.

Requirements

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
Graduate of an accredited nursing program.
Current RN licensure in the state of Missouri and/or Illinois, depending on location.
Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirements).

Nice To Haves

B.S. - Bachelor of Science - Nursing
B.S.N. - Bachelor of Science in Nursing
Clinical Research (1 Year)
Clinical Research
Clinical Research Coordination
Clinical Research Management
Clinical Research Methods
Clinical Research Operations
Clinical Techniques
Critical Thinking
Database Management
Effective Written Communication
Electronic Health Records (EHR)
Interpersonal Relationships
Nursing Fundamentals
Oral Communications
Patient Recruitment
Spreadsheet Software
Statistical Analysis Software (SAS)
Team Collaboration

Responsibilities

Works under the Principal Investigator’s (PI) guidance to meet the research objectives of the project.
Assists with study start-up activities including myIRB applications for initial review, modifications/amendments, continuing reviews and reportable events.
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; organization of source documentation and data entry.
Prepares/submits reportable event reports to sponsor(s), IRB 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.
Provides oversight of administration of medications, study drugs, or study interventions, as appropriate.
Administers investigational products in approved setting.
Educates staff nurses caring for research patients by providing necessary information about the research study including intervention, potential adverse events and required study procedures.
Performs other duties incidental to the work described above.