Clinical Research Coordinator II — Independent Trial Execution

Socket.dev; Mansfield (TX); On-site; USD 70,000 - 110,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator II to independently manage daily trial activities, ensure protocol compliance, and safeguard patient safety across GI, hepatology, obesity, and cardiology studies. The role collaborates with investigators, sponsors, CROs, and internal teams to drive enrollment and high-quality data.

The ideal candidate has 3–5 years of clinical research or healthcare experience, a relevant degree, and familiarity with CTMS/EDC systems.

Qualifications

• 3-5 years of clinical research or healthcare experience required.
• Experience in gastroenterology, hepatology, cardiology preferred.
• CCRC® or CCRP® certification preferred.

Responsibilities

• Coordinate industry-sponsored clinical trials from start-up through closeout with minimal supervision.
• Lead patient recruitment and retention including consent discussions and enrollment tracking.
• Maintain study documentation, source records, CTMS updates, and case report forms.
• Prepare for sponsor, CRO, and regulatory monitoring visits, audits, and inspections.
• Ensure patient safety and regulatory compliance per GCP and HIPAA.

Skills

CTMS

EDC systems

Org & detail

GCP

Education

Associate’s or Bachelor’s degree

Tools

CTMS

EDC systems

Job description

Iterative Health is seeking a Clinical Research Coordinator II to independently manage daily trial activities, ensure protocol compliance, and safeguard patient safety across GI, hepatology, obesity, and cardiology studies. The role collaborates with investigators, sponsors, CROs, and internal teams to drive enrollment and high-quality data.

The ideal candidate has 3–5 years of clinical research or healthcare experience, a relevant degree, and familiarity with CTMS/EDC systems.