Clinical Coordinator

University of Colorado•Hybrid, CO

88d•$49,899 - $69,072•Hybrid

About The Position

Clinical Coordinators perform clinical research related functions which includes research conducted with human subjects. This participant-oriented research includes mechanisms of human disease, therapeutic interventions, clinical trials, or development of new technologies. Clinical Coordinators may also assist with epidemiologic and behavioral studies and/or outcomes research and health services research.

Requirements

A bachelor’s degree in public health, public administration, social/behavioral sciences, physical sciences, nursing, healthcare, finance, accounting, business administration, business, or a directly related field from an accredited institution
A combination of education and related technical/military/paraprofessional experience may be substituted for a bachelor’s degree on a year for year basis.
One (1) year clinical research or related experience
Applicants must meet minimum qualifications at the time of hire.
Applicants must be legally authorized to work in the United States without requiring sponsorship. We are unable to provide work visa sponsorship or employment authorization for this position now or in the future.
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
Organized and able to complete multi-step tasks independently

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)
Experience working with individuals with Down syndrome or other intellectual disability
Demonstrate ability to think conceptually about project design and implementation; anticipate potential problems and study needs
One year of experience working directly with IRB submissions and familiarity with basic regulatory tasks required in a clinical trial.
Two (2) years of clinical research or related experience
English/Spanish bilingual is beneficial
Knowledge of electronic data capture systems (e.g., EMR or HER and data management systems)

Responsibilities

Perform day-to-day operations of clinical trials and studies
Obtain medical history from consented participants, including follow-up for off-site medical records and completion of a participant health survey. Must be able to reliably transcribe orally reported medical history as written notes.
Obtain informed consent and/or assent from study participants and ensure that the process is properly documented, and that informed consent form documents are filed as required.
Schedule subject participation in research clinical trials and coordinate the availability of necessary space and clinical research support (e.g., physician, nurse practitioner, laboratory, radiology, pharmacy).
Adhere to research regulatory standards.
Collect code, and summarize information obtained from research in an accurate and timely manner
Master study materials, including but not limited to protocols, informed consent forms, and all other essential study documents for assigned studies