Independent Clinical Research Coordinator II

Iterative Scopes; San Marcos (TX); On-site; USD 60,000 - 85,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator II to coordinate daily study activities and ensure protocol compliance, patient safety, and data quality across trials. You will work with patients, investigators, sponsors, CROs, and internal teams to drive successful trial execution.

Requirements include a science or healthcare degree and 3–5 years of clinical research experience; gastroenterology/hepatology/cardiology exposure is a plus.

Qualifications

• 3–5 years of clinical research or healthcare experience.
• Experience in gastroenterology, hepatology, or cardiology is preferred.
• Familiarity with CTMS or EDC systems is beneficial.

Responsibilities

• Independently coordinate industry-sponsored clinical trials from start-up through closeout.
• Lead patient recruitment, enrollment tracking, and retention efforts.
• Ensure accurate data entry and timely resolution of data queries.
• Prepare for sponsor, CRO, and regulatory monitoring activities.
• Maintain study documentation and regulatory compliance (GCP, HIPAA).

Skills

Strong organizational skills

Attention to detail

Ability to manage competing priorities

Proficiency with CTMS and EDC systems

Ability to read, interpret, and apply:

Education

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

Tools

CTMS

EDC systems

Job description

Iterative Health is seeking a Clinical Research Coordinator II to coordinate daily study activities and ensure protocol compliance, patient safety, and data quality across trials. You will work with patients, investigators, sponsors, CROs, and internal teams to drive successful trial execution.

Requirements include a science or healthcare degree and 3–5 years of clinical research experience; gastroenterology/hepatology/cardiology exposure is a plus.