Clinical Research Coordinator (Open Rank, Entry to Senior)

University of Colorado•Aurora, CO

2h•Onsite

About The Position

The Clinical Research Coordinator performs clinical research related functions which include research conducted with human subjects or patient-oriented research. This role works with study physicians, ancillary providers, pharmaceutical companies and staff both locally and nationally. The Clinical Research Coordinator is responsible for participant recruiting, consenting, scheduling, performing study visits, processing lab samples, entering data and other study-related duties. This position is a fantastic opportunity to be on the cusp of cutting-edge treatments for rare kidney disease and inflammatory renal illness.

Requirements

Entry Level: Bachelor’s degree in any field.
Intermediate Level: Bachelor’s degree in any field. One (1) year clinical research or related experience. An advanced degree (Masters or PhD) may be substituted for experience on a year-for-year basis if the degree is in a field of study directly related to the work assignment.
Senior Level: Bachelor’s degree in any field. Two (2) years clinical research or related experience. An advanced degree (Masters or PhD) may be substituted for experience on a year-for-year basis if the degree is in a field of study directly related to the work assignment.
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.
Attention to detail and accuracy while maintaining organization of multiple complex projects.

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) or more years of clinical research or related experience.

Responsibilities

Oversee the day-to-day operations of multiple clinical trials and studies from the phase of recruitment to visits to blood/urine processing.
Obtain study subject’s medical history and current medical 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 proper consent process has occurred, is properly documented, and that documents are filed as required .
Educate potential subjects on the details of the studies through phone contacts and personal interviews .
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 .
Collect blood and urine from patients according to the protocol and process and ship out the samples according to the lab manual.