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Iterative Health is a healthcare technology and services company accelerating clinical research to transform patient outcomes. The company operates a performance-driven network of 100+ research sites across the US, Europe, India, and Australia, conducting trials in gastrointestinal, hepatology, obesity, and cardiology. By combining clinical trial expertise with AI, Iterative Health connects pharmaceutical sponsors with high-performing research teams to expedite access to novel therapeutics. The company is headquartered in Cambridge, MA and New York City with 250+ employees worldwide.
As a Clinical Research Coordinator II, you will independently coordinate and manage industry-sponsored clinical trials from start-up through closeout with minimal supervision. You will manage complex study visit schedules, protocol-related activities, and ensure adherence to study timelines and regulatory requirements. Key responsibilities include leading patient recruitment and retention efforts through chart review, patient outreach, informed consent discussions, and enrollment tracking. You will conduct protocol-required patient visits and assessments, perform clinical procedures including vital signs, ECGs, specimen collection, and phlebotomy as permitted by regulations and training. You will process laboratory specimens, maintain accurate and timely study documentation including source records, informed consent forms, CTMS updates, and case report forms, and ensure high-quality data entry with timely resolution of data queries.
You will serve as the primary point of contact for study participants throughout their participation and maintain ongoing communication with sponsors, CROs, investigators, site leadership, and internal teams to proactively resolve issues. You will prepare for and support sponsor, CRO, and regulatory monitoring visits, audits, and inspections, review safety reports, and maintain inventory of study equipment and investigational products. Additional responsibilities include contributing to process improvement initiatives, supporting human research participant protection in compliance with federal regulations and GCP guidelines, and may include onboarding and mentorship of junior research staff.
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
