Entry-Level Clinical Research Coordinator I

Iterative-Health; Memphis (TN); On-site; USD 45,000 - 65,000; Full time

Job summary

Iterative Health in Memphis, TN is seeking a Clinical Research Coordinator I to help execute patient-focused clinical trials. The role supports day-to-day study activities while ensuring protocol compliance, participant safety, and accurate documentation.

You will work with sponsors, CROs, investigators, and internal teams to deliver high-quality research and advance innovative therapies in gastrointestinal, hepatology, obesity, and cardiology areas.

Qualifications

• Associate’s or Bachelor’s degree required in a scientific, healthcare, or related discipline.
• 1–3 years of clinical research or healthcare experience required.
• Must be able to perform blood draw, medical review (BP, height, weight) & EKGs as applicable by state law.
• Strong organizational skills and attention to detail.
• Ability to manage competing priorities in a fast-paced environment.

Responsibilities

• Support the coordination and execution of industry-sponsored clinical trials under the guidance of site leadership and senior research staff.
• Coordinate patient visits, procedures, and study-related activities in accordance with protocol requirements and study timelines.
• Support patient recruitment and retention activities including chart review, patient outreach, scheduling, and informed consent coordination.
• Conduct protocol-required patient visits and assessments in accordance with study protocols, GCP guidelines, and site SOPs.
• Perform protocol-required clinical procedures including vital signs, ECGs, specimen collection, and investigational product accountability, as permitted by applicable regulations, training, and organizational policy.
• Process laboratory specimens and prepare shipments in accordance with protocol requirements and applicable IATA regulations.
• Maintain accurate and timely study documentation including source records, informed consent forms, CTMS updates, and case report forms.
• Ensure high-quality data entry and support timely resolution of data queries.
• Serve as a point of contact for study participants throughout study participation.
• Maintain ongoing communication with sponsors, CROs, investigators, and internal site teams to support study execution.
• Support preparation for sponsor, CRO, and regulatory monitoring visits.
• Maintain inventory and organization of study equipment, supplies, and investigational products.
• Support the protection of human research participants in compliance with federal regulations, GCP, HIPAA, and institutional policies.

Skills

Blood draw

EKGs

Organizational skills

Prioritization

Reading protocols

Office software

Education

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

Tools

CTMS/EDC systems

Job description

Iterative Health in Memphis, TN is seeking a Clinical Research Coordinator I to help execute patient-focused clinical trials. The role supports day-to-day study activities while ensuring protocol compliance, participant safety, and accurate documentation.

You will work with sponsors, CROs, investigators, and internal teams to deliver high-quality research and advance innovative therapies in gastrointestinal, hepatology, obesity, and cardiology areas.