About The Position

Our office conducts clinical trials with patients who have chronic kidney disease, polycystic kidney disease, glomerular disease, and/or hypertension. Many of our trials assess novel therapies in these populations. This position will serve as the coordinator for an ongoing 12-month interventional trial assessing the effects of a glucagon-like peptide 1 receptor agonist (GLP1) vs. placebo in people with autosomal dominant kidney disease. This position will provide support on other trials in our office as needed.

Requirements

  • Bachelor’s degree in any field
  • A combination of education and related professional experience may be substituted for a bachelor’s degree on a year for year basis.
  • One (1) year clinical research or related experience (Intermediate level)
  • Two (2) years clinical research or related experience (Senior level)
  • Knowledge and understanding of federal regulations and Good Clinical Practice (GCP)
  • Ability to communicate effectively, both in writing and orally
  • Ability to establish and maintain effective working relationships with employees at all levels throughout the institution
  • Outstanding customer service skills
  • Knowledge of basic human anatomy, physiology medical terminology
  • Ability to interpret and master complex research protocol information
  • Applicants must be legally authorized to work in the United States without requiring sponsorship.

Nice To Haves

  • Bachelor’s degree in science or health related field
  • Two (2) years of clinical research or related experience (Intermediate level)
  • Three (3) years of clinical research or related experience (Senior level)
  • Experience with electronic data capture systems (e.g. EMR or EHR and data management systems)

Responsibilities

  • Recruiting study participants to various clinical trials
  • Performing participant assessments
  • Maintaining regulatory documents
  • Managing study data
  • Processing participant specimens

Benefits

  • Medical: Multiple plan options
  • Dental: Multiple plan options
  • Additional Insurance: Disability, Life, Vision
  • Retirement 401(a) Plan: Employer contributes 10%25 of your gross pay
  • Vacation Days: 22/year (maximum accrual 352 hours)
  • Sick Days: 15/year (unlimited maximum accrual)
  • Holiday Days: 15/year
  • Tuition Benefit: Employees have access to this benefit on all CU campuses
  • ECO Pass: Reduced rate RTD Bus and light rail service
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