Registered Nurse Clinical Research Nurse Coordinator-Bluhm Cardiovascular Institute

Description

The Clinical Research Nurse Coordinator is a registered professional nurse who demonstrates exemplary clinical research knowledge, has strong communication skills and is responsible for serving as a liaison between Northwestern University (NU) clinical research investigator teams (e.g., investigator initiated trials, sponsor trials) and Northwestern Medicine; a joint collaboration between NMG and the NU Feinberg School of Medicine.

The Clinical Research Nurse Coordinator (CRNC) works collaboratively with the inter‑professional team and peers to ensure appropriate implementation and conduct of clinical research studies throughout the lifecycle of a protocol. The CRNC adheres to the ANA Scope and Standards of Practice of Professional Nursing and the Code of Ethics. The CRNC utilizes the NIH Clinical Research Nurse Domain of Practice and Model of Care.

The CRNC reflects the mission, vision, and values of Northwestern Medicine, adheres to the organization’s Code of Ethics and Corporate Compliance Program, and complies with all relevant policies, procedures, guidelines and all other regulatory and accreditation standards.

Collaborate with a wide range of professionals to disseminate patient care outcomes through publications and presentations, managing all stages of research projects—from feasibility, project conception and approval, data collection, literature review to manuscript submission. Participates in monthly meetings with surgeons and NU research team staff to track progress of projects. Clinical expertise in cardiac surgery (valve and atrial fibrillation procedures) is preferred.

Hours:

Monday-Friday 8:00am-4:30pm

• Leads the coordination and support to Principal Investigator(s).
• Reviews research studies in pre‑submission phase for feasibility of protocol implementation.
• Guides the review, revision, and maintenance of protocols. Assures established protocols meet compliance and regulatory requirements.
• Provides guidance to clinical research nurses on projects related to new research study submissions, utilization reviews, wording/phrasing of medical orders, protocols and workflows.
• Develops and maintains clinical nursing research policies, standard operating procedures, and guidelines.
• Supports the development of projects created in response to research‑related problems and events as identified and reported by staff and research study team members (e.g., events, deviations, corrective and preventative actions).
• Collaborates with Clinical Coordinators, Education Coordinators, and peer CRNCs to orient and train new staff to clinical research.
• Collaborates with Clinical Coordinators, Education Coordinators, and peer CRNCs to identify training needed for clinical research nurses about unfamiliar practices, procedures and medications to ensure patient/subject safety and compliance with protocols and regulatory requirements.
• Escalates research‑related concerns to the appropriate leader or committee.
• Serves as a mentor and role model for communication and collaboration with investigator teams and clinical and technical research practices.
• Supports the clinical research nursing staff during adverse events, emergencies, and difficult clinical situations.
• Provides clinical nursing support to both inpatient and/or outpatient teams as needed as a cross trained resource.

• Current license as a Registered Nurse in the State of Illinois.
• Experience in clinical trials
• BSN
• Minimum of two years related clinical experience.
• CPR‑BLS Certification through the American Heart Association (AHA)

• MSN
• Membership in Professional Nursing Organization
• ACLS Certification in clinical areas where required
• Society of Clinical Research Associates' (SOCRA) or Association of Clinical Research Professionals (ACRP) Certification
• Certification in area of clinical specialty.

Northwestern Medicine is an equal opportunity employer (disability, VETS) and does not discriminate in hiring or employment on the basis of age, sex, race, color, religion, national origin, gender identity, veteran status, disability, sexual orientation or any other protected status.

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