Nurse Researcher

Allina Health • Minneapolis, MN

23d • $36 - $50 • Onsite

About The Position

Allina Health is a not-for-profit health system that cares for individuals, families and communities throughout Minnesota and western Wisconsin. If you value putting patients first, consider a career at Allina Health. Our mission is to provide exceptional care as we prevent illness, restore health and provide comfort to all who entrust us with their care. This includes you and your loved ones. We are committed to providing whole person care, investing in your well-being, and enriching your career. Key Position Details: 1.0 FTE (80 hours per two-week pay period) 8-hour Day shifts, Monday-Friday No weekends Provide on-site support at United Hospital for patients and study coordinators (travel required up to approximately 30%). Occasionally travel to Mercy Hospital to collaborate with the stroke program and study coordinators. Mileage reimbursement available for all eligible travel. Job Description: Coordinates care for patients enrolled in clinical research studies in Health System. Under supervision of senior team members and Research Investigators, ensures research patient care needs meet standards. Coordinates research plan of care, provides education for patients enrolled in study and collaborates with other disciplines to provide direct patient care to study participants.

Requirements

• Bachelor's degree from an accredited nursing program
• 2 to 5 years of experience in clinical practice and/or hospital experience in specialty
• RN - MN Board of Nursing required upon hire
• BLS Tier 1 - Basic Life Support - Multisource required upon hire
• Collaborative Institutional Training Initiative (CITI Program) Certification to be completed within (180 days) of hire (offered through Allina Health)

Nice To Haves

• Certification in nursing specialty preferred

Responsibilities

• Ensure coordination of patient care in accordance with research protocol and regulatory requirements.
• Assist with providing protocol-specific education to investigators, nurses, pharmacy staff and any other staff directly supporting study protocol, to ensure accurate and safe administration of study treatments.
• Provide applicable sections of the study protocol to clinical staff to assist with training.
• Coordinate patient care throughout the research study and follow-up period, and ensure compliance with the study.
• Perform safety monitoring and clinical care in accordance with the protocol.
• Conduct ongoing patient evaluations (in collaboration with clinical team) to assess patients’ treatment toxicity and response.
• Assist investigator in dose modifications according to the protocol.
• Instruct staff on side effect management in accordance with the research protocol.
• Perform data management in accordance with the research protocol.
• Maintain systems for appropriate identification, recruitment, consent, and enrollment/ randomization of eligible patients on clinical research studies.
• Assist with study start-up activities including but not limited to participating in pre-study visits, site initiation visits, protocol-specific training, and investigator meetings.
• Perform screening activities and determine patient eligibility, obtain informed consent, and enroll/ randomize patients into studies.
• Maintain communication appropriate for study patients’ age and other special needs.
• Assist with training and mentoring of research and clinical staff for protocol specific procedures.
• Assist with orientation and mentoring of research staff including clinical research coordinators, and other research staff.
• Contribute to development of quality indicators, data collection, review and recommendations.
• Demonstrate ability to work collaboratively with other members of the team including investigators, research staff, and hospital/clinic and infusion center staff.
• Maintain accurate and complete research drug accountability.
• Maintain study drug inventories at research sites.
• Maintain accurate and complete study drug logs.
• Maintain temperature parameters for study drugs according to manufacturers’ recommendations and sponsor requirements.
• Other duties as assigned.

Benefits

• Medical/Dental
• PTO/Time Away
• Retirement Savings Plans
• Life Insurance
• Short-term/Long-term Disability
• Paid Caregiver Leave
• Voluntary Benefits (vision, legal, critical illness)
• Tuition Reimbursement or Continuing Medical Education as applicable
• Student Loan Support Benefits to navigate the Federal Public Service Loan Forgiveness Program

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level