Clinical Research Coordinator I - Webster, TX

Clinical Research Coordinator I - Webster, TXWebster, TXIterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.As a Clinical Research Coordinator I (CRC I) at Iterative Health you will play an important role in the successful execution of clinical trials and the overall patient research experience. This role supports the coordination of day-to-day study activities while ensuring compliance with protocol requirements, regulatory standards, and patient safety guidelines.The CRC I works closely with patients, sponsors, CROs, investigators, and internal teams to help deliver high-quality clinical research and contribute to the advancement of innovative therapies.Where You'll Drive ImpactSupport the coordination and execution of industry-sponsored clinical trials under the guidance of site leadership and senior research staffCoordinate patient visits, procedures, and study-related activities in accordance with protocol requirements and study timelinesSupport patient recruitment and retention activities including chart review, patient outreach, scheduling, and informed consent coordinationConduct protocol-required patient visits and assessments in accordance with study protocols, GCP guidelines, and site SOPsPerform protocol-required clinical procedures including vital signs, ECGs, specimen collection, and investigational product accountability, as permitted by applicable regulations, training, and organizational policyProcess laboratory specimens and prepare shipments in accordance with protocol requirements and applicable IATA regulationsMaintain accurate and timely study documentation including source records, informed consent forms, CTMS updates, and case report formsEnsure high-quality data entry and support timely resolution of data queriesServe as a point of contact for study participants throughout study participationMaintain ongoing communication with sponsors, CROs, investigators, and internal site teams to support study executionSupport preparation for sponsor, CRO, and regulatory monitoring visitsMaintain inventory and organization of study equipment, supplies, and investigational productsSupport the protection of human research participants in compliance with federal regulations, GCP, HIPAA, and institutional policiesMaintain compliance with all site SOPs, privacy standards, and research protocolsPerform job related duties as requestedWhat You Bring to the TeamAssociate's or Bachelor's degree in a scientific, healthcare, or related discipline required1–3 years of clinical research or healthcare experience requiredMust be able to perform blood draw, medical review (blood pressure, height, weight etc.) & EKGs, as applicable by state lawStrong organizational skills and attention to detailAbility to manage competing priorities in a fast-paced environmentAbility to read, interpret, and apply research protocols and clinic policiesProficiency with standard office software and willingness to learn clinical research systemsFamiliarity with CTMS or EDC systems preferredPhysical RequirementsAbility to sit, stand, and move throughout clinical and office environments for extended periods of timeAbility to lift and move up to 25 pounds as neededAt Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact View email address on click.appcast.io.