CLINICAL TRIAL RESEARCH SPECIALIST

Job Description:

Job Description Your Career. Our Company. Together, We Grow. At Southern Illinois Healthcare (SIH), we realize that in order to provide our surrounding communities with excellent care, we must begin by providing our employees with that same care and appreciation. We offer rich opportunities to develop and grow professionally, an environment of excellence in patient care, and the awareness that everything we accomplish is a direct outgrowth of the superb efforts and dedication of our employees. As a non-profit system of almost 4000 employees, we have won national acclaim for our cancer, cardiac, stroke, bariatric, breast imaging, and rehabilitation services. The Clincial Trial Research Specialist is responsible for the gacilitation and coordination of daily clinical trial activities and plays a critical role in the conduct of the study in order to protect the rights and welfare of research subjects while performing biomedical and social-behavioral research in accordance with Good Clinical Practice research protocols and all federal regulatory standards. The specialist will work collaboratively with the entire clinical research team, Principal Investigators, patients, sponsors, and monitors. $21.32/hr minimum - $31.98/hr maximum (range increases based on education, experience and certifications) Responsibilities Recruits and verifies eligibility of study subjects in compliance with the principles of the Belmont Report, Good Clinical Practice, and federal regulations of OHRP and FDA. Reviews and obtains informed consent and documents process; Schedules and conducts study visits with subjects; Conducts follow-up phone calls with subjects ; Scores test results; Collects survey data and review medical records Consults with nurses and physicians to determine subject eligibility according to protocol requirements; Facilitates communication with and education of investigators, key personnel and subjects to maintain project study flow; Maintains detailed study records. Performs scientific literature searches in support of research; Completes research documents in compliance with current local, state, and federal regulatory guidelines, requirements, laws and research protocols.Participates in outreach to promote clinical research at SIH, including but not limited to outreach to physicians, staff, patients, or community.Identifies, records, reports and follows Adverse Events (AE) and Serious Adverse Events (SAE). Collaborates with investigator to address AE and SAE resolution.Identifies and reports protocol deviations, including corrective action plans.Maintains test article (drug or device) and research supply accountability per protocol and SOP.Occasional overnight travel to attend study training meetings, annual SOCRA or PRIM&R meetings and study audits as necessary (10%). Qualifications Bachelors degree in life sciences, health related administration program, public health, or health sciences.An equivalent combination of education and experience may be considered in lieu of degree.Must complete CITI Human Subjects Research Training before interacting with any participants and must complete continuing education annually or as certification demands.Clinical Research Professional certification within two years of hire.COVID vaccination #PIQresearchPandoLogic. Keywords: Clinical Research Associate (CRA), Location: Carbondale, IL - 62901