Independent Clinical Research Coordinator II

Iterative Scopes; Plano (TX); On-site; USD 55,000 - 75,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator II to manage industry-sponsored trials with minimal supervision. You will coordinate visits, ensure protocol adherence, and maintain regulatory compliance across sites.

In this role you will lead patient recruitment and retention, perform study procedures within scope, and maintain study docs, data entry, and CTMS updates to support timely study milestones. Collaboration with sponsors, investigators, and teams is essential.

Qualifications

• Associate's or Bachelor's degree required.
• 3–5 years of clinical research or healthcare experience required.
• Experience in gastroenterology, hepatology, or cardiology preferred.
• CCR C/C RP or equivalent certification preferred.

Responsibilities

• Independently coordinate industry-sponsored clinical trials from start-up to closeout with minimal supervision.
• Manage complex visit schedules and protocol-related activities to meet timelines.
• Lead patient recruitment and retention, including chart reviews, informed consent discussions, and enrollment tracking.

Skills

Clinical research coordination

CTMS

EDC systems

Attention to detail

Multitasking

Education

Associate's degree

Bachelor's degree

Tools

CTMS software

EDC systems

Microsoft Office

Job description

Iterative Health is seeking a Clinical Research Coordinator II to manage industry-sponsored trials with minimal supervision. You will coordinate visits, ensure protocol adherence, and maintain regulatory compliance across sites.

In this role you will lead patient recruitment and retention, perform study procedures within scope, and maintain study docs, data entry, and CTMS updates to support timely study milestones. Collaboration with sponsors, investigators, and teams is essential.