RN - Clinical Research Coordinator

Sanford Health • Fargo, ND

114d • $27 - $44

About The Position

Sanford Health is one of the largest and fastest-growing not-for-profit health systems in the United States. We’re proud to offer many development and advancement opportunities to our nearly 50,000 members of the Sanford Family who are dedicated to the work of health and healing across our broad footprint. This full time position working Monday through Friday 8:00a-4:30pm. Daily tasks include coordinating with patients, going over research expectations and protocols, data entry and some lab processing. Provides an opportunity to learn daily and contribute to treatments of the future. Enthusiasm for learning required, along with participation in educating patients, physicians, nurses and other personnel to the research process.

Requirements

• Graduate from a nationally accredited nursing program preferred.
• Currently holds an unencumbered RN license with the State Board of Nursing where the practice of nursing is occurring.
• Possess multistate licensure if in a Nurse Licensure Compact (NLC) state.
• Obtain and subsequently maintain required department specific competencies and certifications.

Responsibilities

• Organize complex components of clinical trials, including test ordering, procedure scheduling and insurance pre-authorization for participants.
• Conduct patient assessments for adverse events and assist with or complete study related procedures as detailed in the research protocol.
• Adhere to all levels of institutional, state and federal regulations and established research protocols.
• Collaborate with physician investigators to ensure safe and compliant investigational treatment or intervention and follow-up.
• Attend investigator meetings and coordinate pre-study site visits.
• Monitor enrollment goals and modify recruitment plan as needed.
• Ensure the completion of all screening, eligibility and enrollment procedures.
• Work with pharmacy to dispense study articles and provide subject education.
• Clarify questions and concerns with the investigator and sponsor regarding enrollment goals, sponsor expectations and study procedures.
• Review inclusion/exclusion criteria to assure subject eligibility and review with physician investigator.
• Schedule subjects for follow-up visits to review diaries and questionnaires.
• Ensure appropriate specimen collection, batching and shipping as required.
• Document and maintain all study-related procedures, processes and events.
• Document protocol deviations and exemptions and record accurate and timely data.
• Maintain accurate source documentation for all case report entries and input data for submission.
• Prepare case report forms and source documents for sponsor review.
• Abstract data from medical records, clinic, consultation and referral notes for preparation of study forms and flow sheets.
• Communicate effectively with subjects, research team, Institutional Review Board (IRB) and sponsor representatives.
• Occasional local travel between sites and student supervision may be required.

Benefits

• Collaborative team approach and supportive management team.
• Opportunities for continued learning and professional development.
• Emphasis on employee wellbeing through annual events and team building activities.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Bachelor's degree
• Number of Employees: 5,001-10,000 employees