Clinical Research Coordinator I: Drive Patient-Focused Trials

iterativehealth; Memphis (TN); On-site; USD 52,000 - 76,000; Full time

Job summary

Iterative Health in Memphis, TN, is seeking a Clinical Research Coordinator I to support day-to-day trial activities and ensure compliance with GCP, HIPAA, and protocols. You will work with sponsors, CROs, investigators, and site teams to deliver high-quality research experiences for participants.

Responsibilities include coordinating patient visits, data entry, sample handling, consent processes, and assisting with study documentation and monitoring visits.

Qualifications

• Associate's or Bachelor's degree in a scientific, healthcare, or related field.
• 1–3 years of clinical research or healthcare experience.
• Ability to perform blood draws, EKGs, and basic vitals as allowed by state law.

Responsibilities

• Coordinate patient visits, procedures, and study-related activities per protocol.
• Support patient recruitment, outreach, and informed consent coordination.
• Maintain accurate study documentation and data entry in CTMS/EDC.
• Assist with monitoring visits and regulatory documentation.

Skills

Clinical research

Coordination

Communication

Blood draw / EKGs

Education

Associate's or Bachelor's degree in a scientific/healthcare field

Tools

CTMS

EDC systems

Job description

Iterative Health in Memphis, TN, is seeking a Clinical Research Coordinator I to support day-to-day trial activities and ensure compliance with GCP, HIPAA, and protocols. You will work with sponsors, CROs, investigators, and site teams to deliver high-quality research experiences for participants.

Responsibilities include coordinating patient visits, data entry, sample handling, consent processes, and assisting with study documentation and monitoring visits.