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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 gastroenterology, hepatology, obesity, and cardiology.
As a Clinical Research Coordinator II, you will independently manage industry-sponsored clinical trials from startup through closeout with minimal supervision. You will coordinate complex study visit schedules, lead patient recruitment and retention efforts, and conduct protocol-required patient visits and assessments. Key responsibilities include managing informed consent discussions, enrollment tracking, performing clinical procedures (vital signs, ECGs, specimen collection, phlebotomy), processing laboratory specimens, and maintaining accurate study documentation including source records and case report forms.
You will serve as the primary point of contact for study participants, maintain ongoing communication with sponsors, CROs, investigators, and site leadership, and proactively resolve study-related issues. Additional duties include preparing for sponsor and regulatory monitoring visits, reviewing safety reports, maintaining study equipment and investigational product inventory, and supporting process improvement initiatives. You may mentor junior research staff and contribute to human research participant protection in compliance with federal regulations, GCP, HIPAA, and institutional policies.
Iterative Health is headquartered in Cambridge, Massachusetts and New York City with 250+ employees worldwide.
REQUIREMENTS:
- 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, or 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 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
