RN Research Nurse Coordinator ll - Cardiology

Washington University in St. Louis; St. Louis (MO); In loco; USD 65.000 - 95.000; Tempo pieno

Descrizione del lavoro

Washington University in St. Louis is seeking a Research Nurse Coordinator who will lead a multi-disciplinary research project, coordinate enrollment of study subjects, and ensure adherence to study procedures and protocols.

The role includes supervision of staff and collaboration with sponsors and regulatory bodies. Applicants should have an Associate Degree or Nursing Diploma, RN licensure in IL/MO, and active BLS certification.

Competenze

• RN licensure required (Illinois or Missouri)
• BLS certification required or expected
• 2+ years in nursing and 2+ years in research preferred

Mansioni

• Lead coordination of enrollment and study procedures under PI guidance.
• Ensure IRB submissions and regulatory compliance.
• Oversee data collection, source documentation, and patient care activities.
• Supervise study staff as assigned and train team members.
• Manage study materials, specimens, and adverse event monitoring.

Conoscenze

Clinical Research Coordination

Clinical Research Management

Clinical Research Methods

Clinical Techniques

Database Management

Active Listening

Team Collaboration

Formazione

Associate Degree In Nursing Or Diploma In Registered Nursing

Descrizione del lavoro

Location

SAINT LOUIS, MO 63110

Scheduled Hours

40

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.

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

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

Education

Associate Degree In Nursing Or Diploma In Registered Nursing

Certifications /Professional Licenses

The list below may include all acceptable certifications, professional licenses and issuers. More than one credential, certification or professional license may be required depending on the role.

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.

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 Certification.

Preferred Qualifications

Education

No additional education unless stated elsewhere in the job posting.

Certifications /Professional Licenses

No additional certification/professional licenses unless stated elsewhere in the job posting.

Work Experience

No additional work experience unless stated elsewhere in the job posting.

Skills

Active Listening, Clinical Research Coordination, Clinical Research Management, Clinical Research Methods, Clinical Research Operations, Clinical Techniques, Database Management, De