Coordinate and perform daily clinical research activities in accordance with approved protocols
Assist with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols
Recruit, interview and enroll patients
Obtain informed consent and ensure consent process is administered in compliance
Educate patients and families of purpose, goals, and processes of clinical study
Coordinate scheduling and follow-through of patient care appointments, procedures, & other diagnostic testing in accordance with study protocol
Participate in the collection, processing & evaluation of biological samples
Administer, evaluate and calculate standardized scoring of diagnostic, psychological or behavioral testing or questionnaires
Assist with monitoring patients for adverse reactions to study treatment, procedure or medication
Notify appropriate clinical professional to evaluate patient response
Document unfavorable responses and notify research sponsors & applicable regulatory agencies
Participate in evaluating patients for compliance related to protocol
Assist with collecting, extracting, coding, and analyzing clinical research data
Generate reports and reviews to ensure validity of data
Support activities to ensure compliance with all Institutional Review Boards (IRB), FDA regulations

Bachelor’s Degree in Biological Sciences, Health Sciences, Social Sciences or other medical field, or equivalent combination of education experience required
1 year of relevant experience required
2-4 years of relevant experience preferred
Experience or knowledge in specialty area preferred
Knowledge of medical terminology desired
Clinical research certification from an accredited certifying agency desired
Computer skills required with experience using Microsoft Software applications desired

Clinical Research Coordinator

About this role