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Iterative Health is a healthcare technology and services company that powers clinical research acceleration across a network of 100+ sites in the US, Europe, India, and Australia. The company specializes in gastrointestinal, hepatology, obesity, and cardiology research, combining clinical trial expertise with AI to connect sponsors with high-performing research teams.
As a Clinical Research Coordinator II, you will independently manage industry-sponsored clinical trials from start-up through closeout with minimal supervision. You will coordinate complex study visit schedules, lead patient recruitment and retention efforts including chart review, outreach, informed consent discussions, and enrollment tracking. You will conduct protocol-required patient visits and assessments, perform clinical procedures (vital signs, ECGs, specimen collection, phlebotomy) as permitted by regulations and training, and process laboratory specimens in accordance with IATA regulations.
Key responsibilities include maintaining accurate and timely study documentation (source records, informed consent forms, CTMS updates, case report forms), ensuring high-quality data entry and timely resolution of data queries, and serving as the primary point of contact for study participants. You will maintain ongoing communication with sponsors, CROs, investigators, and site leadership to proactively resolve issues. Additional duties include preparing for and supporting sponsor, CRO, and regulatory monitoring visits and audits; reviewing safety reports; maintaining inventory of study equipment and investigational products; and contributing to process improvement initiatives. You may support 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
