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Clinical Research Nurse 1 – Neuro Sciences / Movement Disorders

Rush University Medical Center

This is a Contract position in Chicago, IL posted July 28, 2019.

Job Title: Clinical Research Nurse 1
– Neuro Sciences / Movement Disorders Department: Shift: 1st Specialty: Research Job Number: 2019-1516 Date Posted: 05/24/2019 Position Type: Nursing-Ambulatory/Outpatient Job Qualifications: At Rush University Medical Center, we are committed to advancing scientific medical knowledge through research.

We are revitalizing our medical centers with an emphasis on productivity, transparency and accountability.

Are you looking to be a part of observational biomarker clinical trials pertaining to Movement Disorders?

Would you like to work with internationally renowned Movement disorder Specialists?

If this describes you, you may be the right candidate for the Clinical Research Nurse 1 position with the Movement Disorders Department.

Position Summary: This position exists under the general direction of the Office of Research Affairs’ Clinical Research Administration Division, their clinical department / division, and in partnership with the Principal Investigator (PI), Co-investigator(s), other study personnel, and sponsoring agents.

The Clinical Research Nurse I conducts clinical research and potentially helps to develop studies and projects.

The Clinical Research Nurse I works with the Principal Investigator for subject recruitment, eligibility, enrollment, informed consent, retention, education, and protocol adherence.

Clinical responsibilities include monitoring toxicities, assessing clinical response and providing exemplary patient care while ensuring the protocol is conducted in a high quality manner.

The Clinical Research Nurse I conducts clinical research in compliance with Rush, State, and Federal guidelines.

In addition, the Clinical Research Nurse I communicates research-related information to patients, families, nursing, and medical staff as necessary.

The individual who holds this position exemplifies the Rush mission, vision and values and acts in accordance with Rush policies and procedures.

Position Responsibilities Include: Adheres to the policies, procedures, and guidelines instituted by Office of Research Affairs and the Office of Research Compliance.

Coordinates clinical research studies conducted by Principal Investigator(s) including, but not limited to grant-funded research, externally sponsored clinical research, and investigator-initiated clinical research conducted on site at Rush or its affiliated sites.

Creates standard research orders.

Evaluates and assesses subject eligibility for inclusion in research protocols (pre-screening, screening, and enrollment).

Obtains informed consent and document according to institutional policy.

Performs subject evaluations, administers medication, and provides nursing support to perform diagnostic, therapeutic, and surgical procedures.

Identifies and communicates process improvements relative to safety monitoring.

Develops and implements procedures for data quality assurance.

Serves as the accountable team member for protocol adherence.

Ensures study team members are performing activities within the established research protocol (as outlined in the Delegation of Authority Log).

Maintains communications (both written and verbal) on a regular schedule with the Investigator and/or the assigned contact.

Communicates with study subject regarding subject procedures and visit schedule.

Works closely with the Clinical Research Administration Division to ensure Standard Operating Procedures (SOPs) are implemented and documented in accordance within study sponsor, Principal Investigator, and regulatory agency specifications.

Updates the Clinical Research Administration Division as necessary.

Performs other duties as assigned.

Position Qualifications Include: Current State of Illinois Registered Nurse licensure.

Bachelor of Science Degree in Nursing required.

A minimum of two years of clinical experience.

Infusion experience required.

Ability to communicate complex regulatory concepts in everyday language.

Ability to develop rapport with a diverse set of individuals and departments.

Demonstrated problem-solving skills with a solution-orientation.

Ability to work both independently and in team settings.

Ability to work flexible hours and travel occasionally to accommodate study and patient schedules.

Demonstrated knowledge of clinical research principles, regulatory requirements, and ethical guidelines preferred.

Utilizes professional judgment and critical decision making skills required to plan for and provide care to research subjects and/or patients.

Strong organizational skills and attention to detail Company Highlights: Ranked among the top academic medical centers in the country, Rush University Medical Center is an outstanding place to enhance your career.

Everything we do centers on one goal: improving patient care.

The Association for the Accreditation of Human Research Protection Programs (AAHRPP) has awarded Rush full accreditation for three years.

Rush is one of the first academic medical centers in Illinois to receive this accreditation.

As an academic medical center, Rush University Medical Center in Chicago, Illinois, is committed to advancing medical knowledge through research.

Investigators at Rush are involved in more than 1,600 projects, including hundreds of clinical studies to test the effectiveness and safety of new therapies and medical devices, as well as to expand scientific and medical knowledge.

RUMC offers a competitive salary, outstanding benefits & the professional advantages of an environment that supports your development & recognizes your achievements.

Rush University is home to one of the first medical colleges in the Midwest and one of the nation’s top-ranked nursing colleges, as well as graduate programs in allied health, health systems management and biomedical research.

Rush University Medical Center is an Equal Opportunity Employer that welcomes and encourages all applicants to apply regardless of age, race, sex, religion, color, national origin, disability, veteran status, sexual orientation, gender identity and/or expression, marital or parental status, ancestry, citizenship status, pregnancy or other reason prohibited by law.

At Rush University Medical Center, we are committed to advancing scientific medical knowledge through research.

We are revitalizing our medical centers with an emphasis on productivity, transparency and accountability.

Are you looking to be a part of observational biomarker clinical trials pertaining to Movement Disorders?

Would you like to work with internationally renowned Movement disorder Specialists?

If this describes you, you may be the right candidate for the Clinical Research Nurse 1 position with the Movement Disorders Department.

Position Summary: This position exists under the general direction of the Office of Research Affairs’ Clinical Research Administration Division, their clinical department / division, and in partnership with the Principal Investigator (PI), Co-investigator(s), other study personnel, and sponsoring agents.

The Clinical Research Nurse I conducts clinical research and potentially helps to develop studies and projects.

The Clinical Research Nurse I works with the Principal Investigator for subject recruitment, eligibility, enrollment, informed consent, retention, education, and protocol adherence.

Clinical responsibilities include monitoring toxicities, assessing clinical response and providing exemplary patient care while ensuring the protocol is conducted in a high quality manner.

The Clinical Research Nurse I conducts clinical research in compliance with Rush, State, and Federal guidelines.

In addition, the Clinical Research Nurse I communicates research-related information to patients, families, nursing, and medical staff as necessary.

The individual who holds this position exemplifies the Rush mission, vision and values and acts in accordance with Rush policies and procedures.

Position Responsibilities Include: Adheres to the policies, procedures, and guidelines instituted by Office of Research Affairs and the Office of Research Compliance.

Coordinates clinical research studies conducted by Principal Investigator(s) including, but not limited to grant-funded research, externally sponsored clinical research, and investigator-initiated clinical research conducted on site at Rush or its affiliated sites.

Creates standard research orders.

Evaluates and assesses subject eligibility for inclusion in research protocols (pre-screening, screening, and enrollment).

Obtains informed consent and document according to institutional policy.

Performs subject evaluations, administers medication, and provides nursing support to perform diagnostic, therapeutic, and surgical procedures.

Identifies and communicates process improvements relative to safety monitoring.

Develops and implements procedures for data quality assurance.

Serves as the accountable team member for protocol adherence.

Ensures study team members are performing activities within the established research protocol (as outlined in the Delegation of Authority Log).

Maintains communications (both written and verbal) on a regular schedule with the Investigator and/or the assigned contact.

Communicates with study subject regarding subject procedures and visit schedule.

Works closely with the Clinical Research Administration Division to ensure Standard Operating Procedures (SOPs) are implemented and documented in accordance within study sponsor, Principal Investigator, and regulatory agency specifications.

Updates the Clinical Research Administration Division as necessary.

Performs other duties as assigned.

Position Qualifications Include: Current State of Illinois Registered Nurse licensure.

Bachelor of Science Degree in Nursing required.

A minimum of two years of clinical experience.

Infusion experience required.

Ability to communicate complex regulatory concepts in everyday language.

Ability to develop rapport with a diverse set of individuals and departments.

Demonstrated problem-solving skills with a solution-orientation.

Ability to work both independently and in team settings.

Ability to work flexible hours and travel occasionally to accommodate study and patient schedules.

Demonstrated knowledge of clinical research principles, regulatory requirements, and ethical guidelines preferred.

Utilizes professional judgment and critical decision making skills required to plan for and provide care to research subjects and/or patients.

Strong organizational skills and attention to detail Company Highlights: Ranked among the top academic medical centers in the country, Rush University Medical Center is an outstanding place to enhance your career.

Everything we do centers on one goal: improving patient care.

The Association for the Accreditation of Human Research Protection Programs (AAHRPP) has awarded Rush full accreditation for three years.

Rush is one of the first academic medical centers in Illinois to receive this accreditation.

As an academic medical center, Rush University Medical Center in Chicago, Illinois, is committed to advancing medical knowledge through research.

Investigators at Rush are involved in more than 1,600 projects, including hundreds of clinical studies to test the effectiveness and safety of new therapies and medical devices, as well as to expand scientific and medical knowledge.

RUMC offers a competitive salary, outstanding benefits & the professional advantages of an environment that supports your development & recognizes your achievements.

Rush University is home to one of the first medical colleges in the Midwest and one of the nation’s top-ranked nursing colleges, as well as graduate programs in allied health, health systems management and biomedical research.

Rush University Medical Center is an Equal Opportunity Employer that welcomes and encourages all applicants to apply regardless of age, race, sex, religion, color, national origin, disability, veteran status, sexual orientation, gender identity and/or expression, marital or parental status, ancestry, citizenship status, pregnancy or other reason prohibited by law.