Open Rank Clinical Research Coordinator (Entry – Intermediate)

University of Colorado•Aurora, CO

1d•Onsite

About The Position

The Renal Research Office conducts clinical trials with patients who have chronic kidney disease, polycystic kidney disease, glomerular disease, hypertension, and/or have had transplants. Many of our trials assess novel therapies in these populations. This position will serve as the coordinator for an ongoing trial taking place at the CTRC and a new study beginning at the CU Medicine Building. Both focus on Kidney Disease in Diabetes.

Requirements

Bachelor’s degree in any field.
One (1) year clinical research or related experience.
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, and medical terminology.
Ability to interpret and master complex research protocol information.
Ability to enter data effectively and efficiently.
Strong interpersonal skills.
Effective organizational and problem-solving skills.
Accountable and ability to take ownership of your tasks and projects.
Experience with Microsoft office programs and emails.
Ability to work independently after training period.

Nice To Haves

Bachelor’s degree in science, psychology, pre-health, sociology, public health, or health related field.
Two (2) years of clinical research or related experience.
Experience with electronic data capture systems (e.g. EMR or EHR and data management systems).
Knowledge of obesity and diabetes physiology.

Responsibilities

Assist with and oversee the day-to-day operations of clinical trials and studies.
Obtain study subject’s medical history and current medication information, reviews research protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial.
Perform informed consent process or ensures that the informed consent process has occurred, is properly documented, and that informed consent form documents are filed as required.
Perform participant assessments.
Schedule subject participation in research clinical trial, coordinating availability of necessary space, and clinical research support (e.g., physician, nurse practitioner, laboratory, radiology, pharmacy).
Collect, code, and analyze data obtained from research in an accurate and timely manner.