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Iterative Health is a healthcare technology and services company accelerating clinical research across gastrointestinal, hepatology, obesity, and cardiology therapeutic areas. The company operates a network of 100+ research sites globally and combines clinical trial expertise with AI to connect pharmaceutical sponsors with high-performing research teams.
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 including chart review, outreach, informed consent, 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 compliance 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. You will prepare for and support sponsor, CRO, and regulatory monitoring visits, audits, and inspections, review safety reports for timely investigator review, and maintain inventory of study equipment and investigational products.
Additional responsibilities include contributing to process improvement initiatives, ensuring compliance with federal regulations, GCP, HIPAA, and institutional policies, 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
