Resarch RN I - Center for Cancer and Blood Disorders
About The Position
Ann & Robert H. Lurie Children’s Hospital of Chicago provides superior pediatric care in a setting that offers the latest benefits and innovations in medical technology, research and family-friendly design. As the largest pediatric provider in the region with a 140-year legacy of excellence, kids and their families are at the center of all we do. Ann & Robert H. Lurie Children’s Hospital of Chicago is ranked in all 10 specialties by the U.S. News & World Report. General Summary of Position Responsibility: This position provides family centered care, understands, and integrates appropriate patient growth and developmental processes into care delivery of patients with acute and chronic diseases, and other disorders with a central focus on safeguarding of research participants. This position also supports study implementation in various settings, including study coordination, data management and integrity, and compliance and reporting of regulatory requirements. Utilizes the nursing process and performs responsibilities aligning with the Magnet® Model. This position contributes to and facilitates clinical research activities in accordance to established guidelines. Assists to identify resources to advance research nursing practice. Performs job functions adhering to service principles with customer service focus of innovation, service excellence and teamwork to provide the highest quality care and service.
Requirements
- Bachelor’s degree in nursing required. For positions that are identified as difficult to fill, CNO may allow approval for hiring of candidates with Associate Degree in nursing with equivalent experience in lieu of BSN or above.
- RN licensure in the state of Illinois
- A minimum of 2 years of clinical experience required or ascended to RN2 competencies; previous pediatric experience preferred.
- GCP and CITI training required within 3 months of hire.
- Basic Life Support Certification required.
- Advanced computer skills in Microsoft Office Suite.
- Strong written and verbal communication skills.
- Excellent organizational and analytical skills. Excellent customer service skills.
- Ability to work in multiple projects simultaneously and under strict deadlines.
Nice To Haves
- Association of Clinical Research Professional (ACRO) Certification and/or Society of Clinical Research Associates (SOCRA) Certification preferred.
Responsibilities
- Supports development of SOPs, screen participants, plans for and conducts participant visits, collects data, and maintains integrity, prepares for study audits and participates in corrective actions, acts as liaison with sponsors, regulatory bodies, and others.
- Assists with Institutional Review Board (IRB) submissions, identification, and consent/enrollment of research study participants.
- Maintains data and follows-up on research participant’s care under supervision of PI/Co-I.
- Maintains regulatory forms, source documents and case report forms in accordance with established guidelines.
- Ensures accuracy, completeness, and integrity of research data, and may be asked to prepare data to assist with data analysis.
- Assists or coordinate with day-to-day operational support of clinical research protocol execution for one (1) PI or division.
- Supports development of SOPs, screens participants, plans for and conducts participant visits, prepares for study audits and participates in corrective actions, acts as liaison with sponsors, regulatory bodies, and others.
- Performs nursing assessments utilizing a variety of assessment methods and/or area-specific tools.
- Assists with the development or individualization of existing plans of care and goals relative to patient and family needs.
- Monitors the health and responses of participants during clinical research studies in conjunction with clinical and study teams.
- Performs physical assessments and vital signs, administers treatments and/or therapies and other research study activities assuring research participant’s safety.
- May delegate tasks and supervise activities of other licensed and unlicensed study personnel.
- Ensure research participants understand risks/benefits of participation and differences between clinical and research activities.
- Identifies and may record adverse events and work with others to assess the appropriate action.
- Liaison with all ancillary research departments (e.g., research lab, pharmacy, etc.) needed for specific research protocols.
- Maintains communication as needed with research participants.
- Responds to queries for data integrity.
- Identifies self-learning needs and creates professional development opportunities to ensure professional goals.
Benefits
- For full time and part time employees who work 20 or more hours per week we offer a generous benefits package that includes:
- Medical, dental and vision insurance
- Employer paid group term life and disability
- Employer contribution toward Health Savings Account
- Flexible Spending Accounts
- Paid Time Off (PTO), Paid Holidays and Paid Parental Leave
- 403(b) with a 5% employer match
- Various voluntary benefits:
- Supplemental Life, AD&D and Disability
- Critical Illness, Accident and Hospital Indemnity coverage
- Tuition assistance
- Student loan servicing and support
- Adoption benefits
- Backup Childcare and Eldercare
- Employee Assistance Program, and other specialized behavioral health services and resources for employees and family members
- Discount on services at Lurie Children’s facilities
- Discount purchasing program
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
