Clinical Research Coordinator II: Lead Trial Ops & Enrollment

Iterative Scopes; Lubbock (TX); On-site; USD 60,000 - 80,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate daily study activities and ensure protocol, regulatory, and patient safety compliance. You will work with patients, investigators, sponsors, CROs, and internal teams to drive accurate trial execution and enrollment success.

Ideal candidates have 3–5 years of clinical research experience, proficiency with CTMS/EDC, and strong organizational skills in a fast-paced environment.

Qualifications

• Associate or Bachelor degree in a scientific, healthcare, or related discipline.
• 3–5 years of clinical research or healthcare experience preferred.
• Experience in gastroenterology, hepatology, cardiology is a plus.

Responsibilities

• Coordinate industry-sponsored clinical trials from start-up to closeout with minimal supervision.
• Manage complex visit schedules and ensure adherence to timelines.
• Lead patient recruitment and retention including chart review and enrollment tracking.
• Conduct patient visits and assessments per protocol and GCP guidelines.
• Perform required procedures and specimen handling per regs and SOPs.
• Maintain study documentation, CTMS updates, and CRFs.
• Ensure data quality and timely data query resolution.
• Serve as a primary point of contact for participants.
• Communicate with sponsors, CROs, investigators, and internal teams.
• Support monitoring visits, audits, and inspections.
• Maintain inventory of study equipment and investigational products.
• Contribute to process-improvement initiatives.
• Support protection of human research participants and compliance.

Skills

Clinical Research

CTMS

EDC

Organization

GCP/HIPAA

Education

Associate or Bachelor in science/healthcare

3-5 years clinical research experience

Tools

CTMS

EDC

Office apps

Job description

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate daily study activities and ensure protocol, regulatory, and patient safety compliance. You will work with patients, investigators, sponsors, CROs, and internal teams to drive accurate trial execution and enrollment success.

Ideal candidates have 3–5 years of clinical research experience, proficiency with CTMS/EDC, and strong organizational skills in a fast-paced environment.