Location: Chicago, Illinois
Business Unit: Rush Medical Center
Hospital: Rush University Medical Center
Department: Res-Recr - Mokhlesi
Work Type: Full Time (Total FTE between 0.9 and 1.0)
Shift: Shift 1
Work Schedule: 8 Hr (9:00:00 AM - 5:30:00 PM) Hours are flexible for start and end times
Rush offers exceptional rewards and benefits learn more at our Rush benefits page (https://www.rush.edu/rush-careers/employee-benefits).
Pay Range: $34.24 - $61.25 per hour
Rush salaries are determined by many factors including, but not limited to, education, job-related experience and skills, as well as internal equity and industry specific market data. The pay range for each role reflects Rush’s anticipated wage or salary reasonably expected to be offered for the position. Offers may vary depending on the circumstances of each case.
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.
The Rush Interdisciplinary Consortium for Critical Care Trials and Data Science (RICCC) consist of Investigators, Clinical Studies Coordinators, Data Managers, Data Engineers, Data Scientists, Biostatisticians, Regulatory Coordinators, and other Nursing Staff. This role will fulfill the traditional research roles of a Clinical Research RN, including but not limited to, eligibility screening, subject recruitment, enrollment, informed consent, retention, education, and protocol adherence. In addition, you will aid with the conduct, regulatory support, data collection, and dataset development/maintenance for a variety of projects related to the care of critically ill patients. To fulfill this role, you will effectively communicate research-related information to patients, families, nursing, and medical staff as necessary. This position supports multiple clinical research studies, which may include multi-centered cooperative group studies, single-site studies, intergroup studies, industry studies, and investigator-initiated studies. The incumbent exemplifies the Rush mission, vision, and values and acts in accordance with Rush policies and procedures.
Other Information
Required Job Qualifications:
- Bachelor’s degree in Nursing (BSN) or Associate’s degree in nursing (ADN)
- Within 1 year from the date of hire, employee must be enrolled in a BSN program.
- RNs hired prior to 10/22/2020 are grandfathered in with an Associate Degree in Nursing (ADN) or diploma in nursing, with no further need to obtain a Bachelor’s degree in Nursing (BAN or BSN).
- Chief Nursing Officer must provide approval for any RNs with ADN degree hired after 10/22/2020, based upon unit need. ADN RNs hired after 10/22/2020 must show continued enrolment towards a BSN degree with a signature of contract stipulating a BSN degree must be completed within 3 years of hire, Failure to do so will result in termination. ADN RNS are not eligible for leveling to RN3.
- 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.
Responsibilities
Job Responsibilities:
RELATIONSHIPS AND CARING
- 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.
- Implements nursing plan of care in connection with study protocol.
- Utilizes clinical assessments to ensure patients receive follow-up care as needed.
- Communicates research-related information to patients, families, nursing and medical staff, including physicians, as necessary.
- Educates the physicians and other clinical staff inpatient and/or outpatient on the study protocol and the plan of care for the research participant.
- Communicates participant health status changes to PI and clinical care staff.
EVIDENCE BASED PRACTICE
- Performs subject assessment, administers medication, and provides nursing support to perform diagnostic, therapeutic and surgical procedures.
- Schedules visits and ensures study related orders are completed for the visit. Including providing patient education regarding tests and/or procedures.
- May enter study related data into appropriate databases.
- May collect, process and ship potentially biohazardous specimens.
TECHNICAL EXPERTISE
- Maintains current knowledge of disease/disorder specific conditions and clinical research trends.
- Attends and participates in study specific training, conferences, and education.
- Adhere to attributable, eligible, contemporaneous, original and accurate (ALCOA) documentation standards.
CRITICAL THINKING
- Assesses subject eligibility for inclusion in research protocols, e.g., pre-screening, screening and enrollment.
- May obtain informed consent and document according to institutional policy.
- Ensures study team is kept up-to-date on the protocol and safety reports received from the study sponsor.
- Maintains written and verbal communications on regular schedule with PI and other assigned contacts.
- May prepare for, participate in routine monitoring visits, audits, etc.
LEADERSHIP
- 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.
- Implements, and communicates process and procedures for data quality assurance and safety monitoring.
- Accountable to PI for protocol adherence. Helps to ensure research team is performing activities within established protocols.
- May provide training to members of the study team and departmental clinical staff related to study protocols, policies and procedures.
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.
