Clinical Research Coordinator II

Iterative-Health; Waterloo (IA); On-site; USD 55,000 - 85,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate industry-sponsored trials, ensure protocol compliance, and support enrollment goals. You will manage visits, perform protocol procedures, maintain study documents, and collaborate with sponsors, CROs, and site teams to drive high-quality trial execution.

You will work closely with investigators and staff to ensure patient safety, accurate data capture, and timely monitoring visits in a fast-paced

Qualifications

• Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline required.
• 3–5 years of clinical research or healthcare experience required.
• CCRC® or CCRP® preferred or equivalent certification.
• Strong organizational skills and attention to detail.
• Ability to manage competing priorities in a fast-paced environment.
• Proficiency with CTMS, EDC systems, and standard office software applications.
• Familiarity with CTMS or EDC systems preferred.

Responsibilities

• Independently coordinate and manage industry-sponsored clinical trials from start-up through closeout with minimal supervision.
• Manage complex study visit schedules and protocol-related activities while ensuring adherence to timelines.
• Lead patient recruitment and retention efforts including chart review, outreach, informed consent discussions, and enrollment tracking.
• Conduct protocol-required patient visits and assessments following GCP and site SOPs.
• Perform protocol-required clinical procedures including vital signs, ECGs, specimen collection, and phlebotomy as allowed.
• Process laboratory specimens and prepare shipments per protocol and IATA rules.
• Maintain accurate study documentation including source records, CRFs, and CTMS updates.
• Ensure high-quality data entry and timely resolution of data queries.
• Serve as a primary contact for study participants and maintain sponsor/site communications.

Skills

Organizational skills

Attention to detail

Multitasking

Protocol interpretation

Education

Bachelor’s or Associate’s degree in a scientific/healthcare field

Tools

CTMS

EDC systems

Office software

Job description

Overview

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. We operate a performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research in communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. The company combines clinical trial expertise with AI to connect sponsors with high-performing research teams that expedite access to novel therapeutics. Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees worldwide.

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 manages complex studies with minimal oversight while collaborating 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
• 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