Clinical Research Coordinator I - RI Academic Affairs & Research Dev-3

Overview With supervision, CRCs engage in enrollment, recruitment, and retention of research participants, and perform other tasks as needed. CRCs conduct clinical interviews for children and adults, obtain mental‑health history, and review reported suicidal ideation/behavior to determine if further intervention is indicated. Studies focus on youth mental health, including school‑based programs. Travel to school research sites is required. Bachelor’s degree in a social science field and prior research or mental‑health field experience is preferred. Effective customer service, communication, organization, and attention to detail are required. Bilingual Spanish/English preferred. Typical hours: Monday‑Friday 8a.m. – 4:30p.m.; one late day per week 12p.m. – 8:30p.m. Hours are subject to change based on project needs. Job Description Summary The Clinical Research CoordinatorI manages elements of a clinical study to meet protocol obligations while following ICH/GCP guidelines and institutional standard operating procedures. Responsibilities include start‑up, launch, day‑to‑day study management and closure activities. Essential Functions Recruit, consent, and enroll subjects in accordance with ICH/GCP regulations and protocol procedures; serve as patient/family advocate. Verify inclusion/exclusion criteria; alert investigators to safety concerns, protocol deviations, or premature termination requests. Collect and manage research data and subject information; maintain accurate data collection for all study data, including laboratory analyses. Prepare and process human specimens; collect blood, urine, and other samples as needed; perform CLIA‑waived laboratory assessments. Complete screening sheets and recruitment logs; create source documents to facilitate systematic data collection and protocol execution. Collaborate, coordinate, and schedule subject study visits with other hospital services and the PI/sub‑PI. Adhere to departmental quality control guidelines; complete Case Report Forms (CRFs) as instructed by the sponsor and maintain regulatory binder and documents. Education Requirements Associate’s degree, STNA, PCA, LPN, MA, or equivalent work‑related experience required. BA/BS preferred. Licensure Requirements Not specified. Certifications Ability to obtain CRA/CRC certification in a timely manner. Skills Understanding of medical terminology and clinical research preferred. Working knowledge of PCs, 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. Experience Previous experience in clinical research or a health‑care related field preferred. Physical Requirements Occasionally: cold temperatures, fumes/gases/vapors, loud noises, reaching above shoulder, squatting/kneeling. Frequently: bending/twisting, biohazard waste, blood and/or bodily fluids, chemicals/medications, communicable diseases/pathogens; lifting/carrying 0‑10lbs, 11‑20lbs, 21‑40lbs; machinery/patient equipment; pushing/pulling 0‑25lbs, 26‑40lbs, 41‑60lbs, 61‑100lbs; sitting, standing, walking. Continuously: audible speech, computer skills, decision making, depth perception, neck flexion/extension, hand use (grasping, gripping, turning), hearing acuity, data interpretation, peripheral vision, problem solving, repetitive hand/arm use, seeing (far/near). EOE M/F/Disability/Vet #J-18808-Ljbffr 10 Nationwide Children's Hospital