Clinical Research Coordinator I (PA/NJ Residents Only)

What you’d do

Coordinate clinical trials by recruiting, screening, enrolling, and following up with subjects per protocol. Review protocols and consent forms, obtain consent, and extract data from medical charts. Full-time position in Bethlehem, PA. Found on the employer's careers page on Oct 22, 2026. Apply through the link.

You’ll need

• Knowledge of ICH/GCP guidelines
• HIPPA Regulations and Confidentiality Policies
• Experience with clinical trial conduct
• Ability to review protocols and consents
• Physical ability to sit, stand, and occasionally lift up to 25 pounds