Senior CRC: Lead Trials & Mentorship

Iterative Health; Lubbock (TX); On-site; USD 75,000 - 110,000; Full time

Job summary

Iterative Health in the United States seeks a Senior Clinical Research Coordinator to oversee complex industry-sponsored trials, from start-up through closeout, ensuring study timelines and regulatory compliance.

You will coordinate visits, lead recruitment and retention efforts, mentor junior staff, manage data and documentation in CTMS/EDC systems, and collaborate with sponsors, CROs, investigators, and site leadership to drive study success.

Qualifications

• Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline.
• 5+ years of clinical research or healthcare experience.
• Must be able to perform blood draw, EKGs, and related assessments as allowed by state law.
• CCRC® or CCRP® certification strongly preferred.
• Strong understanding of GCP, FDA regulations, and clinical research operations.

Responsibilities

• Lead and independently manage complex industry-sponsored clinical trials from start-up to closeout.
• Coordinate protocol visits, timelines, and regulatory requirements.
• Lead patient recruitment and retention initiatives to support enrollment.
• Mentor junior coordinators and staff on trial processes and sponsor communication.
• Perform protocol-required patient visits and assessments per GCP and SOPs.
• Maintain study documentation and data quality including CTMS updates.

Skills

Clinical research

GCP compliance

Regulatory knowledge

Mentoring

CTMS

EDC

Communication

Organization

Education

Bachelor's degree in science/healthcare

Tools

CTMS

EDC systems

Microsoft Office

Job description

Iterative Health in the United States seeks a Senior Clinical Research Coordinator to oversee complex industry-sponsored trials, from start-up through closeout, ensuring study timelines and regulatory compliance.

You will coordinate visits, lead recruitment and retention efforts, mentor junior staff, manage data and documentation in CTMS/EDC systems, and collaborate with sponsors, CROs, investigators, and site leadership to drive study success.