Open Rank Clinical Research Coordinator (Entry – Senior)
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 interventional trial assessing the impact of intramuscular muscle strength training (IMST) on systolic blood pressure in adults with chronic kidney disease. This position will provide support to other trials in our office as needed. This position offers the opportunity to conduct clinical research participant visits with the potential to impact standard of care practices. There are options to learn various technical skills depending on the candidate’s interest and the current needs of the research. Various trials in our office involve assessment of patient vascular function to evaluate the impact of a given intervention on CKD-related cardiovascular dysfunction and kidney disease progression.
Requirements
- Entry Level: Bachelor’s degree in any field.
- Intermediate Level: Bachelor’s degree in any field. One (1) year of clinical research or related experience.
- Senior Level: Bachelor’s degree in any field. Two (2) years clinical research or related experience.
- A combination of education and related technical/military/paraprofessional experience may be substituted for a bachelor’s degree on a year for year basis.
- Applicants must meet minimum qualifications at the time of hire.
- 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.
Nice To Haves
- Bachelor’s degree in science or health related field.
- Experience with electronic data capture systems (e.g. EMR or EHR and data management systems).
- Three (3) years of clinical research or related experience.
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% of your gross pay
- Paid Time Off: Accruals over the year
- 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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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
