Clinical Research Nurse Coordinator
About The Position
The Clinical Research Nurse Coordinator (CRNC) is a registered professional nurse who applies clinical research expertise and strong communication skills while serving as a liaison between Northwestern University clinical research investigator teams and Northwestern Memorial Hospital. The role works collaboratively with interprofessional teams and peers to support the appropriate implementation and conduct of clinical research studies throughout each protocol’s lifecycle. The CRNC follows professional nursing standards and ethics, the NIH Clinical Research Nurse Domain of Practice and Model of Care, and applicable organizational, regulatory, and accreditation requirements. The position provides coordination and support to principal investigators, reviews studies for implementation feasibility, guides protocol development and maintenance, and supports compliance, quality improvement, and staff education. It also provides clinical nursing support to inpatient and/or outpatient teams as needed and participates in assigned committees and task forces.
Requirements
- Current Illinois Registered Nurse license as a Professional Nurse.
- Bachelor of Science in Nursing (BSN).
- At least two years of related clinical experience.
- Experience in clinical trials.
- Certification in area of clinical specialty.
- CPR-BLS certification through the American Heart Association (AHA).
Nice To Haves
- Master of Science in Nursing (MSN).
- Membership in a professional nursing organization.
- ACLS certification in clinical areas where required.
- Certification from the Society of Clinical Research Associates (SOCRA) or the Association of Clinical Research Professionals (ACRP).
Responsibilities
- Lead coordination and support for Principal Investigator(s).
- Review research studies during the pre-submission phase for feasibility of protocol implementation.
- Guide the review, revision, and maintenance of protocols and ensure established protocols meet compliance and regulatory requirements.
- Guide clinical research nurses on new study submissions, utilization reviews, medical-order wording and phrasing, protocols, and workflows.
- Develop and maintain clinical nursing research policies, standard operating procedures, and guidelines.
- Review and trend research-related deviations and workflow events; report findings to the Manager and Inter-professional Quality Committee and recommend actions to ensure compliance.
- Support projects developed in response to research-related problems and events reported by staff and research study team members, including events, deviations, and corrective and preventative actions.
- Collaborate with Clinical Coordinators, Education Coordinators, and peer CRNCs to orient and train new staff in clinical research.
- Collaborate with Clinical Coordinators, Education Coordinators, and peer CRNCs to identify training needs for clinical research nurses regarding unfamiliar practices, procedures, and medications to promote patient/subject safety and compliance.
- Escalate research-related concerns to the appropriate leader or committee.
- Serve as a mentor and role model for communication and collaboration with investigator teams and for clinical and technical research practices.
- Support clinical research nursing staff during adverse events, emergencies, and difficult clinical situations.
- Provide clinical nursing support to inpatient and/or outpatient teams as needed as a cross-trained resource.
- Participate in unit, departmental, divisional, or hospital committees and task forces as assigned.
- Remain clinically proficient within area of expertise.
Benefits
- Tuition reimbursement
- Loan forgiveness
- 401(k) matching
- A wide range of benefits supporting physical, emotional, and financial well-being and protection for unexpected life events
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
