Strong fit for candidates with 3-5 years of clinical research experience who can independently manage complex studies and coordinate across multiple stakeholders in gastrointestinal, hepatology, cardiology, or obesity domains.
Derived from job-description analysis by Serendipath's career intelligence engine.
Original posting from Iterative Health via Greenhouse
Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.
We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.
As a Clinical Research Coordinator II (CRC II) at Iterative Health you will play a critical role in the successful execution of clinical trials by independently coordinating daily study activities and ensuring compliance with protocol requirements, regulatory standards, and patient safety guidelines.
This role is responsible for managing complex studies with minimal oversight while partnering closely with patients, investigators, sponsors, CROs, and internal teams to drive high-quality study execution and enrollment success.
Where You’ll Drive Impact
Independently coordinate and manage industry-sponsored clinical trials from study start-up through closeout with minimal supervision
Manage complex study visit schedules and protocol-related activities while ensuring adherence to study timelines and requirements
Lead patient recruitment and retention efforts including chart review, patient outreach, informed consent discussions, and enrollment tracking to support study enrollment goals
Conduct protocol-required patient visits and assessments in accordance with study protocols, GCP guidelines, and site SOPs
Perform protocol-required clinical procedures including vital signs, ECGs, specimen collection, investigational product accountability, and phlebotomy, as permitted by applicable regulations, training, and organizational policy
Process laboratory specimens and prepare shipments in accordance with protocol requirements and applicable IATA regulations
Maintain accurate, complete, and timely study documentation including source records, informed consent forms, CTMS updates, and case report forms
Ensure high-quality data entry and timely resolution of data queries in accordance with sponsor expectations and established timelines
Serve as a primary point of contact for study participants throughout study participation
Maintain ongoing communication with sponsors, CROs, investigators, site leadership, and internal teams to proactively resolve study-related issues
Prepare for and support sponsor, CRO, and regulatory monitoring visits, audits, and inspections
Review safety reports and ensure appropriate investigator review and documentation in a timely manner
Maintain inventory and organization of study equipment, supplies, and investigational products onsite
Contribute to process improvement initiatives to enhance site performance, operational efficiency, and patient experience
Support the protection of human research participants in compliance with federal regulations, GCP, HIPAA, and institutional policies
Maintain compliance with all site SOPs, privacy standards, and research protocols
May support onboarding and mentorship of junior research staff and coordinators
Perform job related duties as requested
What You Bring to the Team
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, 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 Requirements
Ability to sit, stand, and move throughout clinical and office environments for extended periods of time
Ability to lift and move up to 25 pounds as needed
At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.