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Iterative Health is a healthcare technology and services company that accelerates clinical research to improve patient outcomes. The company operates a network of 100+ research sites across the US, Europe, India, and Australia, conducting trials in gastrointestinal, hepatology, obesity, and cardiology. They combine clinical trial expertise with AI to connect pharmaceutical sponsors with high-performing research teams.
As a Clinical Research Coordinator I, you will support the day-to-day execution of clinical trials while ensuring compliance with protocols, regulatory standards, and patient safety. You will work with patients, sponsors, CROs, investigators, and internal teams to deliver high-quality clinical research.
Key responsibilities include:
- Coordinate and execute industry-sponsored clinical trials under site leadership guidance
- Manage patient visits, procedures, and study activities according to protocol requirements
- Support patient recruitment and retention through chart review, outreach, scheduling, and informed consent
- Conduct protocol-required patient visits and assessments following GCP guidelines and site SOPs
- Perform clinical procedures including vital signs, ECGs, specimen collection, and investigational product accountability
- Process laboratory specimens and prepare shipments per protocol and IATA regulations
- Maintain accurate study documentation including source records, informed consent forms, CTMS updates, and case report forms
- Ensure high-quality data entry and support resolution of data queries
- Serve as primary contact for study participants
- Communicate with sponsors, CROs, investigators, and internal teams
- Prepare for sponsor, CRO, and regulatory monitoring visits
- Maintain inventory 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 draws, medical reviews (blood pressure, height, weight), and EKGs as permitted 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
