Clinical Research Coordinator (Open Rank: Entry-Intermediate)

University of Colorado

6d•$48,446 - $67,061•Hybrid

About The Position

Entry and Intermediate Clinical Science Professionals perform clinical research related functions, which may include patient-oriented research or research conducted with human subjects. Patient-oriented research includes mechanisms of human disease, therapeutic interventions, clinical trials, or development of new technologies. Entry and Intermediate Clinical Science Professionals may also assist with epidemiologic and behavioral studies and/or outcomes research and health services research.

Requirements

Bachelor’s degree in any field
A combination of education and related technical/paraprofessional experience may be substituted for the bachelor’s degree on a year for year basis
Two (2) years of clinical research or related experience (Intermediate Level)

Nice To Haves

Bachelor’s degree in science or health related field
Clinical research or related experience
Experience with using electronic data capture systems (e.g. Electronic Medical Record (EMR) or Electronic Health Record (EHR) and data management systems)
Experience with study visits (e.g. consenting/assenting participants, providing questionnaires, performing protocol-related activities)
Knowledge and understanding of federal regulations and Good Clinical Practice (GCP)
Ability to communicate effectively, both in writing and orally
Outstanding customer service skills
Demonstrated commitment and leadership ability to advance diversity and inclusion
Knowledge of basic human anatomy, physiology medical terminology
Ability to interpret and master complex research protocol information

Responsibilities

Assist with and oversee the day-to-day operations of clinical trials and research studies
Serves as the Primary Coordinator on multiple trials/studies
Participate in subject recruitment efforts, including communicating with patients expressing an interest and all pre-screening/screening activities
Perform informed consent process or ensures that the informed consent process has occurred, is properly documented, and that informed consent documents are filed as required
Interact with participants to gather study data and/or specimens
Schedule participant participation in research clinical trials, coordinating availability of necessary space, and clinical research support (e.g., physician, nurse practitioner, laboratory, radiology, pharmacy)
Obtain study participants’ medical history and current medication information, reviews research protocol inclusion/exclusion criteria, and confirms eligibility of participant to participate in the clinical trial
Responsible for overseeing the secure handling, distribution, and tracking of gift cards, ensuring compliance with institutional policies and accurate record-keeping
Create/maintain research databases in REDCap, Excel, Sponsor’s Electronic Data Capture (EDC) system, and OnCore
Collect, code, and analyze data obtained from research in an accurate and timely manner
Assist faculty with writing research protocols
Write informed consents/assents, IRB applications, and related documents in compliance with IRB requirements, and to manage the full approval process.