Clinical Research Coordinator II: Drive Trials & Enrollment

Iterative Scopes; Cary (NC); On-site; USD 65,000 - 90,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate industry-sponsored clinical trials from start-up through closeout with minimal supervision. You will manage complex visit schedules, lead patient recruitment, and ensure protocol adherence under GCP and SOPs.

The role requires 3–5 years of clinical research or healthcare experience, a scientific/healthcare degree, and CTMS/EDC proficiency.

Qualifications

• Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline.
• 3-5 years of clinical research or healthcare experience.
• Gastroenterology, hepatology, or cardiology experience preferred.
• CCRC or CCRP certification preferred.
• Proficiency with CTMS and EDC systems.

Responsibilities

• Coordinate industry-sponsored clinical trials from start-up to closeout with minimal supervision.
• Manage complex visit schedules and protocol activities to meet timelines.
• Lead patient recruitment and retention, including chart review and enrollment tracking.
• Conduct protocol-required visits and assessments per GCP and SOPs.
• Prepare for sponsor, CRO, and regulatory monitoring visits and inspections.
• Maintain study documentation and data entry with timely query resolution.
• Maintain inventory of study equipment and investigational products onsite.
• Support onboarding and mentorship of junior staff.

Skills

Clinical research experience

CTMS proficiency

EDC proficiency

Organizational skills

Prioritization

Attention to detail

Education

Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline

Tools

CTMS

EDC systems

Job description

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate industry-sponsored clinical trials from start-up through closeout with minimal supervision. You will manage complex visit schedules, lead patient recruitment, and ensure protocol adherence under GCP and SOPs.

The role requires 3–5 years of clinical research or healthcare experience, a scientific/healthcare degree, and CTMS/EDC proficiency.