Clinical Research Coordinator

Location
Michigan, United States
Posted
06 Dec 2018
End of advertisement period
10 Dec 2018
Ref
165636
Contract Type
Permanent
Hours
Part Time

Job Summary

This position involves coordinating and conducting clinical research concerning neurogenic bowel with subjects with physical disabilities. The person in this position will maintain and amend the IRB; file ORIOs/AEs as necessary; recruit and screen potential participants; collect data via interviews and medical records abstraction; maintain study documentation; and coordinate with investigators and other study staff.

Responsibilities*

  • Maintain and amend IRB and insure that study activities comply; file ORIOs/AEs as necessary
  • Recruit, screen and enroll potential subjects and document in study databases
  • Maintain manual of procedures and protocol documents
  • Communicate with investigators and other study staff about progress and prepare progress reports
  • Required Qualifications*
  • Experience reviewing medical records and conducting interviews with medical populations
  • Experience with data entry and management and able to learn new electronic data systems
  • Familiarity with IRBs
  • Ability to readily learn new terminology
  • Good writing skills
  • Bachelors' degree in related field and/or RN

Desired Qualifications*

  • Experience with clinical research;
  • Background in medical field, such as nursing, therapy, or social work;
  • Familiarity with electronic data systems (i.e., REDCap) and experience with MiChart;
  • Experience (personal or professional) with spinal cord injury;
  • Knowledge about disability including neurogenic bladder

Work Schedule

Weekdays: Days
Work Locations: Ann Arbor, MI

Additional Information

Please note; this is a term-limited appointment.  At the end of the term, the appointment will terminate and will not be eligible for Reduction in Force (RIF) benefits.

U-M EEO/AA Statement

The University of Michigan is an equal opportunity/affirmative action employer.