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Iterative Health is a healthcare technology and services company that powers clinical research acceleration across a network of 100+ sites in the US, Europe, India, and Australia. The company combines clinical trial expertise with AI to connect pharmaceutical sponsors with high-performing research teams, focusing on gastrointestinal, hepatology, obesity, and cardiology research.
As a Clinical Research Coordinator I, you will support the day-to-day execution of industry-sponsored clinical trials while ensuring compliance with protocol requirements, regulatory standards, and patient safety guidelines. You will work closely with patients, sponsors, CROs, investigators, and internal teams to deliver high-quality clinical research.
Key responsibilities include:
- Coordinate and execute clinical trial activities under guidance of site leadership and senior research staff
- Coordinate patient visits, procedures, and study-related activities in accordance with protocol requirements and timelines
- Support patient recruitment and retention through chart review, outreach, scheduling, and informed consent coordination
- Conduct protocol-required patient visits and assessments following study protocols, GCP guidelines, and site SOPs
- Perform clinical procedures including vital signs, ECGs, specimen collection, and investigational product accountability as permitted by regulations and training
- Process laboratory specimens and prepare shipments per protocol requirements and IATA regulations
- Maintain accurate and timely study documentation including source records, informed consent forms, CTMS updates, and case report forms
- Ensure high-quality data entry and support timely resolution of data queries
- Serve as primary point of contact for study participants throughout their participation
- Maintain ongoing communication with sponsors, CROs, investigators, and internal teams
- Support preparation for sponsor, CRO, and regulatory monitoring visits
- Maintain inventory and organization of study equipment, supplies, and investigational products
- Support 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
Requirements:
- Associate's or Bachelor's degree in a scientific, healthcare, or related discipline (required)
- 1–3 years of clinical research or healthcare experience (required)
- Ability to perform blood draws, medical reviews (blood pressure, height, weight, etc.), and EKGs as applicable by state law (required)
- 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 standard office software and willingness to learn clinical research systems
- Familiarity with CTMS or EDC systems (preferred)
- Physical ability to sit, stand, and move throughout clinical and office environments for extended periods
- Physical ability to lift and move up to 25 pounds as needed
