Clinical Research Coordinator I — Trials & IRB Liaison

Baptist; Memphis (TN); On-site; USD 42,000 - 60,000; Full time

Job summary

Baptist Memphis is seeking a Research Coordinator I to coordinate study protocols, recruit and screen participants, and manage data per the research plan. You will liaise with the IRB, sponsors, and investigators to uphold quality and regulatory compliance.

The role requires familiarity with medical terminology, EMR systems, and CTMS, with travel possible to support multi-site activities. Accommodations for professional development will be considered.

Qualifications

• High School Diploma required.
• Associate’s Degree or equivalent experience preferred.
• Knowledge of Medical Terminology (training).

Responsibilities

• Coordinate and manage human subjects research in accordance with GCP and regulations.
• Submit and report to the IRB; ensure compliance and documentation.

Skills

Organizational skills

Attention to detail

Education

High School Diploma

Associate’s Degree or equivalent experience

Tools

EMR

Clinical Trials Management System

Job description

Baptist Memphis is seeking a Research Coordinator I to coordinate study protocols, recruit and screen participants, and manage data per the research plan. You will liaise with the IRB, sponsors, and investigators to uphold quality and regulatory compliance.

The role requires familiarity with medical terminology, EMR systems, and CTMS, with travel possible to support multi-site activities. Accommodations for professional development will be considered.