Part-Time Clinical Research Coordinator - On-Site 16 hrs/wk

IQVIA; Brownsville (TX); Presencial; USD 48.000 - 58.000; A tiempo parcial

Descripción de la vacante

IQVIA is seeking a part-time Clinical Research Coordinator in Brownsville, TX to support clinical studies under a principal investigator. The role includes hands-on procedures, patient interactions, and ensuring GCP compliance.

You will manage data entry, CRFs, and EDC queries, contributing to high-quality clinical data and patient safety. The position emphasizes on-site responsibilities with a focus on accurate data collection, patient advocacy, and collaboration with study teams.

Formación

• Bachelor’s degree or equivalent; 1+ year in clinical research.
• Experience with GCP and medical terminology.
• Proficiency with EDC and data entry processes.

Responsabilidades

• Perform clinical procedures, including ECGs, sample collection, and vital signs.
• Coordinate studies and ensure adherence to study protocols and GCP guidelines.
• Conduct patient study visits and support participants throughout the research process.
• Prepare study materials, set up equipment, and plan logistical activities.
• Recruit, screen, and orient patients based on inclusion/exclusion criteria while ensuring safety.
• Enter and maintain data in CRFs and EDC systems.
• Assist with EDC query management and data quality improvements.
• Collaborate with investigators, sponsors, and monitors to address study issues.
• Advocate for patients and maintain a safe environment per Health & Safety policies.

Conocimientos

GCP knowledge

Clinical data management

Patient interactions

Educación

Bachelor's degree or equivalent

Herramientas

EDC systems

Descripción del empleo

IQVIA is seeking a part-time Clinical Research Coordinator in Brownsville, TX to support clinical studies under a principal investigator. The role includes hands-on procedures, patient interactions, and ensuring GCP compliance.

You will manage data entry, CRFs, and EDC queries, contributing to high-quality clinical data and patient safety. The position emphasizes on-site responsibilities with a focus on accurate data collection, patient advocacy, and collaboration with study teams.