Clinical Coordinator (Open Rank: Entry - Intermediate)
About the position 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 • Obtain informed consent and/or assent from study participants and ensure proper documentation • Schedule subject participation in research clinical trials and coordinate necessary clinical research support • Adhere to research regulatory standards • Collect, code, and summarize information obtained from research in an accurate and timely manner • Master study materials, including protocols and informed consent forms for assigned studies Requirements • A bachelor's degree in any field from an accredited institution (Entry Professional) • A bachelor's degree in any field from an accredited institution and one year of clinical research or related experience (Intermediate Professional) • A combination of education and related technical/paraprofessional experience may substitute for the bachelor's degree on a year-for-year basis • Knowledge of basic human anatomy, physiology, and medical terminology • Ability to interpret and master complex research protocol information Nice-to-haves • Bachelor's degree in science or health-related field • Experience with electronic data capture systems (e.g., EMR or EHR) • Experience working with individuals with Down syndrome or other intellectual disabilities • Bilingual, English/Spanish beneficial • Two years of experience working as a clinical coordinator or in a directly related role Benefits • Health insurance • Life insurance • Retirement plans • Tuition benefits • ECO pass • Paid time off - vacation, sick, and holidays Apply tot his job