Independent Clinical Research Coordinator II

Iterative Health

Plainview (TX)

Presencial

USD 55.000 - 85.000

Jornada completa

Hace 3 días

Sé de los primeros/as/es en solicitar esta vacante

Consigue una respuesta de este empleador

Tu currículum y tu carta de presentación, adaptados exactamente a lo que buscan contratar.

Supera los filtros ATS

Descripción de la vacante

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate daily study activities and ensure protocol compliance, safety standards, and data integrity. You will partner with patients, investigators, sponsors, CROs, and internal teams to drive enrollment and high-quality execution.

The role requires 3–5 years in clinical research or healthcare, a science/healthcare degree, and familiarity with CTMS/EDC.

Formación

Requires an Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline.
3–5 years of clinical research or healthcare experience.
Experience in gastroenterology, hepatology, or cardiology is preferred.
CCR C/CCRP or equivalent certification preferred.
Strong organizational skills and attention to detail.

Responsabilidades

Independently coordinate and manage industry-sponsored clinical trials from start-up through closeout with minimal supervision.
Lead patient recruitment and retention, including chart review, outreach, informed consent, and enrollment tracking.
Conduct protocol-required patient visits and assessments per GCP guidelines and site SOPs.
Perform protocol-required clinical procedures and vitals, ECGs, phlebotomy where permitted.
Maintain accurate study documentation, CTMS updates, and data queries per sponsor timelines.
Support site leadership, sponsors, CROs, and internal teams to resolve issues proactively.
Prepare for sponsor, CRO, and regulatory monitoring visits and inspections.