Clinical Research Coordinator II - Houston, TX

requirements and applicable IATA regulations Maintain accurate, complete, and timely study documentation including source records, informed consent forms, CTMS updates, and case report forms Ensure high-quality data entry and timely resolution of data queries in accordance with sponsor expectations and established timelines Serve as a primary point of contact for study participants throughout study participation Maintain ongoing communication with sponsors, CROs, investigators, site leadership, and internal teams to proactively resolve study-related issues Prepare for and support sponsor, CRO, and regulatory monitoring visits, audits, and inspections Review safety reports and ensure appropriate investigator review and documentation in a timely manner Maintain inventory and organization of study equipment, supplies, and investigational products onsite Contribute to process improvement initiatives to enhance site performance, operational efficiency, and patient experience Support the protection of human research participants in compliance with federal regulations, GCP, HIPAA, and institutional policies Maintain compliance with all site SOPs, privacy standards, and research protocols May support onboarding and mentorship of junior research staff and coordinators Perform job related duties as requested What You Bring to

the Team Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline required 3-5 years of clinical research or healthcare experience required Experience in [gastroenterology, hepatology, cardiology] therapeutic areas preferred CCRC® — Certified Clinical Research Coordinator or CCRP® — Certified Clinical Research Professional or equivalent clinical research certification preferred Strong organizational skills and attention to detail Ability to manage competing priorities in a fast-paced environment Ability to read, interpret, and apply research protocols and clinic policies Proficiency with CTMS, EDC systems, and standard office software applications Familiarity with CTMS or EDC systems preferred Physical

Requirements Ability to sit, stand, and move throughout clinical and office environments for extended periods of time Ability to lift and move up to 25 pounds as needed At 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 [email protected].

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