Clinical Research Coordinator II: Lead High-Impact Trials

TAU Ventures; Oxford (MS); On-site; USD 65,000 - 85,000; Full time

Job summary

Iterative Health, a healthcare technology and services company, seeks a CRC II to coordinate industry-sponsored clinical trials from start-up to closeout, ensuring compliance with protocol, GCP, and regulatory standards. You will lead patient recruitment and manage complex visit schedules, collaborating with sponsors, CROs, and investigators to drive enrollment and data quality.

The role emphasizes protecting human research participants, maintaining study documentation, and contributing to

Qualifications

• Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline is required.
• 3–5 years of clinical research or healthcare experience is required.
• Experience in gastroenterology, hepatology, or cardiology is preferred.
• CCR CCRC or CCRP certification is preferred.
• Strong organizational skills and attention to detail are essential.
• Ability to manage competing priorities in a fast-paced environment.

Responsibilities

• Independently coordinate and manage industry-sponsored clinical trials from start-up through closeout with minimal supervision.
• Manage complex study visit schedules and protocol-related activities while ensuring timelines.
• Lead patient recruitment and retention efforts including chart review, informed consent discussions, and enrollment tracking.
• Conduct protocol-required patient visits and assessments per protocol, GCP, and SOPs.
• Perform protocol-required clinical procedures, specimen handling, and phlebotomy as permitted by regulations.
• Maintain accurate study documentation including source records, CRFs, and CTMS updates.
• Ensure high-quality data entry and timely resolution of data queries per sponsor timelines.
• Serve as primary contact for study participants and maintain communication with sponsors, CROs, investigators, and internal teams.

Skills

Organizational skills

Attention to detail

Prioritization

Reading protocols

Education

Associate or Bachelor degree in science/healthcare

Tools

CTMS

EDC systems

Microsoft Office

Job description

Iterative Health, a healthcare technology and services company, seeks a CRC II to coordinate industry-sponsored clinical trials from start-up to closeout, ensuring compliance with protocol, GCP, and regulatory standards. You will lead patient recruitment and manage complex visit schedules, collaborating with sponsors, CROs, and investigators to drive enrollment and data quality.

The role emphasizes protecting human research participants, maintaining study documentation, and contributing to