Clinical Research Coordinator II - Trial Leadership

Iterative Scopes; Providence (RI); On-site; USD 65,000 - 90,000; Full time

Job summary

Iterative Health seeks a Clinical Research Coordinator II to independently coordinate industry-sponsored clinical trials from start-up to closeout. You will manage complex visit schedules, lead recruitment and retention, and ensure protocol adherence and data integrity in a fast-paced environment.

You will collaborate with investigators, sponsors, CROs, and internal teams to drive high-quality study execution while maintaining regulatory compliance and patient safety.

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.
• Experience in gastroenterology, hepatology, or cardiology preferred.
• CCR CCRC/CCRP or equivalent certification preferred.
• Strong organizational skills and attention to detail.
• Ability to manage competing priorities in a fast-paced environment.
• Ability to read and apply research protocols and clinic policies.
• Proficiency with CTMS, EDC systems, and standard office software.

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 to meet timelines.
• Lead patient recruitment and retention efforts, including chart review, outreach, informed consent discussions, and enrollment tracking.
• Conduct protocol-required patient visits and assessments per study protocols and GCP.
• Perform protocol-required clinical procedures and specimen handling as allowed by regulations.
• Maintain study documentation, CTMS updates, and case report forms.
• Ensure high-quality data entry and timely resolution of data queries.
• Serve as primary contact for study participants and maintain sponsor/CRO communication.
• Support sponsor, CRO, and regulatory monitoring visits, audits, and inspections.
• Maintain inventory of study equipment and investigational products onsite.

Skills

CTMS proficiency

EDC systems

Organizational skills

Attention to detail

Communication skills

Multitasking

Education

Associate's or Bachelor's degree in science/healthcare

Tools

CTMS

EDC systems

Job description

Iterative Health seeks a Clinical Research Coordinator II to independently coordinate industry-sponsored clinical trials from start-up to closeout. You will manage complex visit schedules, lead recruitment and retention, and ensure protocol adherence and data integrity in a fast-paced environment.

You will collaborate with investigators, sponsors, CROs, and internal teams to drive high-quality study execution while maintaining regulatory compliance and patient safety.