Clinical Research Coordinator I - RI Biobeh Fox

Nationwide Children's Hospital•Columbus, OH

10d•Onsite

About The Position

Dr. Kristen Fox seeks a Clinical Research Coordinator to join her research program focused on health behaviors, psychosocial functioning, and healthcare experiences of youth with congenital heart disease. The coordinator will support a randomized clinical trial evaluating a digital health intervention and other research. This position requires in-person work. During active recruitment and data collection, flexibility to work approximately 4 hours/week during evenings and weekends is required to accommodate family schedules. The position is available immediately.

Requirements

Associate's Degree, or equivalent certification or experience, required.
CNA, PCA, LPN, MA, or equivalent education or experience, required.
Clinical Research Associate (CRA) or Clinical Research Coordinator (CRC) certification after hire, required.
Understanding of medical terminology and clinical research preferred.
Working knowledge of PCs and word processing and data management software
Demonstrated analytical skills with accuracy and attention to detail.
Excellent verbal and written communication skills.
Goal-oriented and self-directive
Strong organizational and interpersonal skills.
Ability to actively participate as a team player.

Nice To Haves

Bachelor's Degree, preferred.
Previous experience in clinical research or health care related field preferred.

Responsibilities

Manages elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines; and departmental/institutional standard operating procedures.
Recruits, consents and enrolls subjects according to ICH/GCP regulations, and subjects’ rights through institutional IRB, federal and state regulations; answers questions related to the protocol procedure as applicable; acts as a patient/family advocate.
Ensures that the subject meets inclusion/exclusion criteria; alerts the investigator when the subject’s safety is in jeopardy, there is a protocol deviation, or when the subject requests premature study termination.
Collects and manages research data and subject information; and maintains accurate data collection of all study data; including laboratory analytical procedures.
Prepares and processes human specimens for use in research studies.
Collects blood, urine, and other samples as needed according to skill level and certifications.
Performs CLIA waived laboratory assessments.
Completes screening sheets and recruitment logs.
Creates source documents that facilitate systematic data collection and/or aid in protocol execution and management and record keeping; and conducts accurate and timely subject data collection.
Collaborates, coordinates, and schedules subject study visits with other hospital services and the PI/sub-I.
Adheres to departmental quality control guidelines.
Completes Case Report Forms (CRFs) as instructed by the sponsor; ensures CRF’s are completed prior to monitoring visits.
Maintains regulatory binder and documents.