Clinical Research Coordinator II — Patient-Centric Trial Lead

Iterative Health; Memphis (TN); Presencial; USD 60 000 - 85 000; Tempo integral

Resumo da oferta

Iterative Health in Memphis, TN is seeking a Clinical Research Coordinator II to independently coordinate daily study activities for industry-sponsored trials, ensuring protocol compliance and patient safety. This role requires collaboration with investigators, sponsors, CROs, and internal teams to drive high-quality study execution.

The ideal candidate has 3–5 years of clinical research or healthcare experience, an appropriate science degree, and familiarity with CTMS/EDC systems.

Qualificações

• Associate or bachelor’s degree in a scientific or healthcare field.
• 3–5 years of clinical research or healthcare experience.
• Gastroenterology, hepatology, or cardiology experience preferred.
• CRCs/CCRP or equivalent certification preferred.

Responsabilidades

• Coordinate industry-sponsored trials from start-up through closeout with minimal supervision.
• Manage complex visit schedules and protocol activities to meet timelines.
• Lead patient recruitment and retention, including informed consent discussions.
• Conduct protocol visits and assessments per GCP and site SOPs.
• Perform clinical procedures and specimen handling as allowed.
• Maintain study documentation and timely data entry with queries.
• Prepare for monitoring visits, audits, and inspections.
• Mentor junior staff and coordinators as needed.

Conhecimentos

Clinical research

Study coordination

CTMS / EDC

Attention to detail

Formação académica

Associate’s or Bachelor’s degree

Ferramentas

CTMS

EDC systems

Office software

Descrição da oferta de emprego

Iterative Health in Memphis, TN is seeking a Clinical Research Coordinator II to independently coordinate daily study activities for industry-sponsored trials, ensuring protocol compliance and patient safety. This role requires collaboration with investigators, sponsors, CROs, and internal teams to drive high-quality study execution.

The ideal candidate has 3–5 years of clinical research or healthcare experience, an appropriate science degree, and familiarity with CTMS/EDC systems.