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Iterative Health is a healthcare technology and services company accelerating clinical research across gastrointestinal, hepatology, obesity, and cardiology. The company operates a network of 100+ research sites globally and combines clinical trial expertise with AI to connect sponsors with high-performing research teams. Headquartered in Cambridge, MA and New York City with 250+ employees worldwide.
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:
- Support coordination and execution of industry-sponsored clinical trials under site leadership guidance
- Coordinate patient visits, procedures, and study-related activities per 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 and IATA regulations
- Maintain accurate and timely study documentation including source records, ICFs, CTMS updates, and case report forms
- Ensure high-quality data entry and support resolution of data queries
- Serve as point of contact for study participants throughout participation
- Maintain 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
- Ensure compliance with federal regulations, GCP, HIPAA, and institutional policies
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 draw, medical review (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
