Clinical Research Coordinator II - Lead Trials & Enrollment

Iterative Scopes; Fort Worth (TX); On-site; USD 70,000 - 95,000; Full time

Job summary

Iterative Health seeks a Clinical Research Coordinator II to independently coordinate complex industry-sponsored trials from start-up to closeout, ensuring adherence to protocol, GCP, and patient safety standards.

You will manage visit schedules, lead patient recruitment, perform visits and assessments, maintain study documentation, and collaborate with sponsors, CROs, investigators, and internal teams to drive high-quality trial execution.

Qualifications

• Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline required.
• 3-5 years of clinical research or healthcare experience required.
• Experience in gastroenterology, hepatology, cardiology therapeutic areas preferred.
• CCRC® — Certified Clinical Research Coordinator or CCRP® — Certified Clinical Research Professional or equivalent clinical research certification preferred.
• Strong organizational skills and attention to detail.
• Ability to manage competing priorities in a fast-paced environment.
• Ability to read, interpret, and apply research protocols and clinic policies.
• Proficiency with CTMS, EDC systems, and standard office software applications.
• Familiarity with CTMS or EDC systems preferred.

Responsibilities

• Coordinate industry-sponsored clinical trials from start-up to closeout with minimal supervision.
• Manage complex study visit schedules and protocol-related activities to meet timelines and requirements.
• Lead patient recruitment and retention including chart review, patient outreach, informed consent discussions, and enrollment tracking.
• Conduct protocol-required patient visits and assessments in accordance with study protocols, GCP and SOPs.
• Maintain study documentation including source records, informed consent forms, CTMS updates, and case report forms.
• Ensure high-quality data entry and timely resolution of data queries.
• Serve as a primary point of contact for study participants and maintain communication with sponsors, CROs, investigators, and internal teams.
• Prepare for and support sponsor, CRO, and regulatory monitoring visits, audits, and inspections.

Skills

Organizational skills

Attention to detail

Time management

Communication

Education

Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline

Tools

CTMS

EDC systems

Office software

Job description

Iterative Health seeks a Clinical Research Coordinator II to independently coordinate complex industry-sponsored trials from start-up to closeout, ensuring adherence to protocol, GCP, and patient safety standards.

You will manage visit schedules, lead patient recruitment, perform visits and assessments, maintain study documentation, and collaborate with sponsors, CROs, investigators, and internal teams to drive high-quality trial execution.