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Key Position Details:

• Remote work - 20%
• Travel Required- 5%
• Day time business hours
• Fully benefit eligible
• IATA training provided by Allina Health

Job Description:

Principle 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.

Job Requirements

• Bachelor's degree in an accredited nursing program required
• 2 to 5 Years experience in clinical practice and/or hospital experience in specialty required
• RN - MN Board of Nursing required Upon Hire
• BLS Tier 1 - Basic Life Support - Multisource required Upon Hire
• International Air Transport Association (IATA) within 180 Days required
• Certification in specialty in nursing specialty preferred

Physical Demands
Sedentary:
Lifting weight Up to 10 lbs. occasionally, negligible weight frequently