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Iterative Health is a healthcare technology and services company accelerating clinical research through a network of 100+ research sites across the US, Europe, India, and Australia. The company combines clinical trial expertise with AI to connect pharmaceutical sponsors with high-performing research teams conducting trials in gastrointestinal, hepatology, obesity, and cardiology.
As a Clinical Research Coordinator I, you will support the day-to-day execution of industry-sponsored clinical trials while ensuring compliance with protocols, 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:
- Coordinating patient visits, procedures, and study-related activities according to protocol requirements and timelines
- Supporting patient recruitment and retention through chart review, outreach, scheduling, and informed consent coordination
- Conducting protocol-required patient visits and assessments, including vital signs, ECGs, and specimen collection
- Maintaining accurate and timely study documentation including source records, informed consent forms, CTMS updates, and case report forms
- Processing laboratory specimens and preparing shipments in accordance with IATA regulations
- Ensuring high-quality data entry and supporting resolution of data queries
- Serving as a point of contact for study participants throughout their participation
- Maintaining communication with sponsors, CROs, investigators, and internal teams
- Supporting preparation for monitoring visits
- Managing study equipment, supplies, and investigational product inventory
- Ensuring 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 draws, medical review (blood pressure, height, weight), 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
- Ability to lift and move up to 25 pounds as needed
