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Iterative Health is a healthcare technology and services company that powers clinical research acceleration across a network of 100+ sites globally. The company combines deep clinical trial expertise with AI to connect pharmaceutical sponsors with high-performing research teams conducting trials in gastrointestinal, hepatology, obesity, and cardiology therapeutic areas.
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, patient outreach, and informed consent discussions. You'll conduct protocol-required patient visits and assessments, perform clinical procedures (vital signs, ECGs, specimen collection, phlebotomy as permitted), and maintain accurate study documentation including source records, informed consent forms, CTMS updates, and case report forms.
Key responsibilities include ensuring high-quality data entry and timely resolution of data queries, serving as the primary point of contact for study participants, maintaining ongoing communication with sponsors, CROs, investigators, and site leadership to resolve issues proactively. You will prepare for and support sponsor, CRO, and regulatory monitoring visits and audits, review safety reports for timely investigator review, and maintain inventory of study equipment and investigational products. You may also support onboarding and mentorship of junior research staff.
This role requires strong organizational skills, attention to detail, and the ability to manage competing priorities in a fast-paced environment. You must be able to read, interpret, and apply research protocols and clinic policies, with proficiency in CTMS, EDC systems, and standard office software. Physical requirements include the ability to sit, stand, and move throughout clinical and office environments for extended periods, and lift up to 25 pounds as needed.
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)
- Proficiency with CTMS, EDC systems, and standard office software applications
- Familiarity with CTMS or EDC systems (preferred)
