RN Research Nurse Coordinator ll - Cardiology

Washington University in St. Louis

St. Louis (MO)

On-site

USD 65,000 - 90,000

Full time

14 days+

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Job summary

Washington University in St. Louis is seeking a nurse coordinator to lead a research project, coordinating enrollment of study subjects and ensuring adherence to the protocol and source documentation.

The role may involve supervising staff and collaborating with multidisciplinary teams to protect human subjects and maintain research integrity. Responsibilities include start-up activities, regulatory submissions, data collection, and coordinating specimen handling and case reporting, with

Qualifications

  • Associate Degree in Nursing or Diploma in Registered Nursing.
  • Basic Life Support (BLS) certification required.
  • Registered Nurse licensure in Illinois and Missouri where applicable.

Responsibilities

  • Lead the research project under PI guidance to meet objectives.
  • Coordinate study start-up activities including regulatory submissions and budget review.
  • Provide direct patient care, document data, and assist physicians.
  • Screen and enroll study subjects and ensure adherence to protocol.

Education

Associate Degree In Nursing Or Diploma In Registered Nursing

Job description

Position Summary

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 1.

Location

SAINT LOUIS, MO 63110

Scheduled Hours

40

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
  • 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

The above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all job duties performed by the personnel so classified. Management reserves the right to revise or amend duties at any time.

Required Qualifications

Associate Degree In Nursing Or Diploma In Registered Nursing

Certifications / Professional Licenses
  • 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

Research (2 Years), Nursing (2 Years)

Skills

Not Applicable

Driver's License

A driver's license is not required for this position.

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