Clinical Research Nurse 1
1 month ago
Hospital: RUSH University Medical Center
Department: Cancer Center-Res Fac
Work Type: Full Time (Total FTE between 0.9 and 1.0)
Shift: Shift 1
Work Schedule: 8 Hr (8:00:00 AM - 5:00:00 PM)
Summary:
A licensed nurse, who, as part of a research team, will provide clinical care within the context of a clinical research study. Under direction of the PI, assists with subject recruitment, eligibility, informed consent and protocol adherence. Monitors research participants for changes in health status, including monitoring toxicities, assessing clinical response and providing exemplary patient care while ensuring the protocol is conducted in a high-quality manner. Educates clinical staff and physicians regarding study. Updates clinical staff on study medications or changes in status, and may administer study medications. Exemplifies the Rush mission, vision and ICARE values and acts in accordance with Rush policies and procedures.
Responsibilities:
Job Responsibilities:
RELATIONSHIPS AND CARING
1. Provides nursing care to patients participating in clinical research studies, may include: standard of care procedures, research procedures, study medication administration and adherence assessments, adverse event assessment documentation, blood draw, EKG administration, and various clinical assessments.
2. Implements nursing plan of care in connection with study protocol.
3. Utilizes clinical assessments to ensure patients receive follow-up care as needed.
4. Communicates research-related information to patients, families, nursing and medical staff, including physicians, as necessary.
5. Educates the physicians and other clinical staff inpatient and/or outpatient on the study protocol and the plan of care for the research participant.
6. Communicates participant health status changes to PI and clinical care staff.
EVIDENCE BASED PRACTICE
7. Performs subject assessment, administers medication, and provides nursing support to perform diagnostic, therapeutic and surgical procedures.
8. Schedules visits and ensures study related orders are completed for the visit. Including providing patient education regarding tests and/or procedures.
9. May enter study related data into appropriate databases.
10. May collect, process and ship potentially biohazardous specimens.
TECHNICAL EXPERTISE
11. Maintains current knowledge of disease/disorder specific conditions and clinical research trends.
12. Attends and participates in study specific training, conferences, and education.
13. Adhere to attributable, eligible, contemporaneous, original and accurate (ALCOA) documentation standards.
CRITICAL THINKING
14. Assesses subject eligibility for inclusion in research protocols, e.g., pre-screening, screening and enrollment.
15. May obtain informed consent and document according to institutional policy.
16. Ensures study team is kept up-to-date on the protocol and safety reports received from the study sponsor.
17. Maintains written and verbal communications on regular schedule with PI and other assigned contacts.
18. May prepare for, participate in routine monitoring visits, audits, etc.
LEADERSHIP
19. Collaborates with PI, sponsor, medical monitor, compliance, staff, Office of Research Affairs and manager to identify and improve routine processes as it relates to the regulatory and operational aspects of a research study.
20. Implements, and communicates process and procedures for data quality assurance and safety monitoring.
21. Accountable to PI for protocol adherence. Helps to ensure research team is performing activities within established protocols.
22. May provide training to members of the study team and departmental clinical staff related to study protocols, policies and procedures.
Other information:
Required Job Qualifications:
• Bachelor of Science in Nursing (BSN) or Master of Science in Nursing (MSN).
• Current IL RN license.
• Basic Life Support certification for Healthcare Professionals.
• Two years of clinical nursing practice experience required.
• Able to demonstrate introductory knowledge of Good Clinical Practices and/or Good Documentation Practices, human subjects protections, institutional, local, state and federal guidelines and regulations related to clinical research with probationary period.
• Ability to communicate complex clinical and regulatory concepts in layperson language.
• Ability to build rapport with diverse patients and peers.
• Demonstrated problem-solving, critical decision makings and professional judgment.
• Strong organizational skills and attention to detail.
• Ability to work successfully both independently and in team settings.
• Flexible work hours and travel may be required.
Preferred Job Qualifications:
• Two years of experience in clinical research as appropriate to study population.
• Clinical specialty certification as appropriate to study population.
Rush is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.
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