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Clinical Research Coordinator

2 months ago

Saint Paul, United States Artius Solutions Full time
Job DescriptionJob Description

Job Title: Clinical Research Coordinator

Facility: Health East Med Research Inst

Location: 45 W 10th St., St. Paul, MN 55102

Schedule: Business hours, Monday through Friday (40 hours per week with potential overtime as needed)

Position Type: 20 Weeks

Clinical Research Coordinator Research Professional 2Responsible for screening, enrolling, and consenting participants in hospital-based COVID-19 research involving a variety of disciplines at the University of Minnesota. Serves as an initial point of contact for COVID-19 clinical research trials happening at Bethesda and St. Joseph's Hospitals. (Duties do not include direct interaction with COVID-19-positive patients.) Uses research and good clinical practice (GCP) knowledge to support investigators in conducting responsible clinical research. This is a 6-month temporary position with the possibility of extension, depending on needs of the COVID-19 research teams. Candidates with varying identities and backgrounds are encouraged to apply.Required Qualifications
  • Bachelor's degree in a health-related field plus 2 years of work experience in research; or a combination of related education and work experience in research totaling 6 years. Experience must include 2 years of coordinator experience.
  • Ability to work independently, make decisions, problem solve, and prioritize duties across multiple clinical studies.
  • Possess excellent communication skills; verbal and written.
  • Completed CITI training
  • Willingness to work on COVID-19 clinical trials
  • Willingness to work 4 10 hour shifts per week including some weekend shifts.
**Proof of non-active tuberculosis and immunization for or resistance to measles, mumps, rubella, Hepatitis B, pertussis, and influenza are required.Preferred Qualifications
  • Experience working in a hospital setting
  • Familiarity with the University of Minnesota, University of Minnesota Medical Center Fairview hospital, and clinics
  • Experience with EPIC
  • Certification as a Clinical Research Coordinator, or qualified to sit the for the certification exam
  • Experience prioritizing among competing deadlines, tasks, and projects
**A background check will be completed by the University of Minnesota Medical Center Fairview as a condition of employment in this position.Essential Functions of Job Duties
  • Manage subject participation in research protocol:
    • Screen potential subjects.
    • Determine subject eligibility, and maintain compliance with protocol eligibility requirements.
    • Work with the study teams to enroll patients.
    • Ensure informed consent and compliance with HIPAA requirements.
    • Obtain or confirm the subject's consent to participate in research. Assess the subject's understanding of the research process, procedures, and plan; implement and conduct subject and family education in response to identified needs.
    • Support study logistics.
  • Demonstrate effective and efficient communication with hospital physicians, nurses, and other health team members.
  • Contribute to the efficiency and effectiveness of the research process by offering suggestions and participating as an active member of the research team.
  • Follow Good Clinical Practice (GCP) guidelines in the conduct, performance, and recording of clinical research.
  • Maintain accurate and complete study records.
  • Track subject data in TASCS and OnCore. Document as required in EPIC.
  • Report work time on an electronic time card.
  • Update Subject Tracking Forms in the organization's business system.
  • Collaborate with other disciplines involved in the research process.

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