Clinical Research Coordinator I — Patient-Centered Trials

Iterative Health; Memphis (TN); On-site; USD 52,000 - 70,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator I in Memphis, TN to assist with day-to-day trial activities and patient experience. You will coordinate visits, ensure protocol adherence, manage documentation, and support data integrity within a fast-paced research environment.

The role requires 1–3 years of clinical research experience, ability to perform blood draws and ECGs, and strong organizational skills to manage competing priorities.

Qualifications

• 1–3 years of clinical research or healthcare experience
• Ability to perform blood draws, vital signs, and ECGs
• Ability to read and apply study protocols and clinic policies

Responsibilities

• Support coordination and execution of industry-sponsored trials under site leadership
• Coordinate patient visits, procedures, and study activities per protocol timelines
• Assist in patient recruitment and retention through chart review and outreach
• Conduct protocol-required patient visits and assessments per GCP and SOPs
• Perform protocol-required procedures including vital signs, ECGs, and specimen handling
• Process laboratory specimens and shipments per protocol and IATA rules
• Maintain accurate study documentation including source records and CTMS updates
• Ensure high-quality data entry and timely data query resolution
• Act as primary contact for study participants during participation
• Maintain communication with sponsors, CROs, investigators and internal teams
• Prepare for sponsor, CRO, and regulatory monitoring visits
• Maintain inventory of study equipment and investigational products
• Support protection of human subjects per federal regs, HIPAA, and policies
• Comply with site SOPs and privacy standards

Skills

Blood draw

Vital signs

ECGs

Data entry

Informed consent

Education

Science/Healthcare degree

Tools

CTMS

EDC

Job description

Iterative Health is seeking a Clinical Research Coordinator I in Memphis, TN to assist with day-to-day trial activities and patient experience. You will coordinate visits, ensure protocol adherence, manage documentation, and support data integrity within a fast-paced research environment.

The role requires 1–3 years of clinical research experience, ability to perform blood draws and ECGs, and strong organizational skills to manage competing priorities.