Clinical Research Coordinator II — Trial Execution

TAU Ventures; San Marcos (TX); On-site; USD 55,000 - 75,000; Full time

Job summary

Iterative Health is a healthcare technology and services company accelerating clinical research to improve patient outcomes. The CRC II will independently coordinate daily study activities, ensuring protocol compliance and patient safety, while collaborating with sponsors, CROs, investigators, and internal teams.

The role requires leading patient recruitment, conducting protocol-required visits, and maintaining high-quality study documentation and data integrity, with a focus on enrollment

Qualifications

• Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline.
• 3–5 years of clinical research or healthcare experience.
• Experience in gastroenterology, hepatology, or cardiology preferred.
• CCRC® or CCRP® or equivalent certification preferred.
• Proficiency with CTMS, EDC systems, and standard office software.

Responsibilities

• Coordinate industry-sponsored clinical trials from start-up through closeout with minimal supervision.
• Manage complex visit schedules and protocol-related activities.

Skills

Organizational skills

Prioritization

Communication

Team collaboration

Patient-focused

Education

Bachelor’s or Associate’s in science/healthcare

Clinical research experience

Tools

CTMS

EDC systems

Job description

Iterative Health is a healthcare technology and services company accelerating clinical research to improve patient outcomes. The CRC II will independently coordinate daily study activities, ensuring protocol compliance and patient safety, while collaborating with sponsors, CROs, investigators, and internal teams.

The role requires leading patient recruitment, conducting protocol-required visits, and maintaining high-quality study documentation and data integrity, with a focus on enrollment