Clinical Research Coordinator II — Lead High-Impact Trials

Iterative Scopes; Memphis (TN); On-site; USD 55,000 - 75,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate industry-sponsored clinical trials across multiple sites. You will manage patient visits, ensure protocol adherence, and drive enrollment while collaborating with sponsors, CROs, investigators, and internal teams.

The role emphasizes data integrity, regulatory compliance (GCP, HIPAA), and on-site trial activities, with opportunities to mentor junior staff.

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, or cardiology preferred.

Responsibilities

• Independently coordinate and manage industry-sponsored clinical trials from start-up through closeout.
• Manage complex visit schedules and protocol-related activities to meet timelines.
• Lead patient recruitment and retention including chart review, outreach, consent discussions, and enrollment tracking.

Skills

Organization

Communication

CTMS

EDC

HIPAA

GCP

Education

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

Tools

CTMS

EDC systems

Office software

Job description

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate industry-sponsored clinical trials across multiple sites. You will manage patient visits, ensure protocol adherence, and drive enrollment while collaborating with sponsors, CROs, investigators, and internal teams.

The role emphasizes data integrity, regulatory compliance (GCP, HIPAA), and on-site trial activities, with opportunities to mentor junior staff.