Rush University Medical Center
Clinical Research Nurse - Cancer Center
Rush University Medical Center, Chicago, Illinois, United States, 60290
Job Description
Location:
Chicago, IL 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) Rush offers exceptional rewards and benefits. Learn more at our Rush benefits page. Summary: A licensed nurse, who, as part of a research team, will provide clinical care within the context of a clinical research study. Under the 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 the 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. 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-making, 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: 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. 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. 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. 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 the study team is kept up-to-date on the protocol and safety reports received from the study sponsor. Maintains written and verbal communications on a regular schedule with PI and other assigned contacts. May prepare for, participate in routine monitoring visits, audits, etc. 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 processes and procedures for data quality assurance and safety monitoring. Accountable to PI for protocol adherence. Helps to ensure the 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. Position:
Clinical Research Nurse - Cancer Center Location:
US:IL:Chicago Req ID:
14256
#J-18808-Ljbffr
Chicago, IL 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) Rush offers exceptional rewards and benefits. Learn more at our Rush benefits page. Summary: A licensed nurse, who, as part of a research team, will provide clinical care within the context of a clinical research study. Under the 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 the 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. 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-making, 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: 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. 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. 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. 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 the study team is kept up-to-date on the protocol and safety reports received from the study sponsor. Maintains written and verbal communications on a regular schedule with PI and other assigned contacts. May prepare for, participate in routine monitoring visits, audits, etc. 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 processes and procedures for data quality assurance and safety monitoring. Accountable to PI for protocol adherence. Helps to ensure the 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. Position:
Clinical Research Nurse - Cancer Center Location:
US:IL:Chicago Req ID:
14256
#J-18808-Ljbffr