Clinical Research Coordinator II - Bariatric GI Trials

10 John C. Lincoln Medical Center; Scottsdale (AZ); Sur place; USD 65 000 - 90 000; Plein temps

Résumé du poste

HonorHealth Research Institute in Scottsdale is seeking a Coordinator-Clinical Research II to manage day-to-day execution of clinical trials and provide clinical data support in compliance with FDA, ICH, and GCP guidelines.

The role collaborates with research staff to collect, verify, and maintain data, handle data forms, and assist with study startup/close-out while ensuring regulatory documentation and quality checks are met.

Qualifications

• 2 years of progressively responsible clinical/clinical research or data management experience required
• Knowledge of ICH/GCP and FDA regulations for clinical trials preferred
• Strong writing and computer skills (Word, Excel, Access, EDC) preferred

Responsabilités

• Manages day-to-day execution of clinical trials and provides clinical data support for the conduct of trials
• Collects, verifies, organizes, and records clinical information in accordance with FDA, ICH, and GCP guidelines
• Performs data management tasks including recruitment support, source document review, data collection, and query resolution
• Supports protocol administration, site initiation, interim monitoring, and study close-out visits as needed
• Precepts and trains staff on data management procedures and systems

Connaissances

Clinical data management

Project management

Regulatory knowledge

Documentation

MS Word

Formation

Health Science degree or 4 years health science-related experience

Outils

MS Word

Excel

Access

EDC (electronic data capture)

Description du poste

HonorHealth Research Institute in Scottsdale is seeking a Coordinator-Clinical Research II to manage day-to-day execution of clinical trials and provide clinical data support in compliance with FDA, ICH, and GCP guidelines.

The role collaborates with research staff to collect, verify, and maintain data, handle data forms, and assist with study startup/close-out while ensuring regulatory documentation and quality checks are met.