Job Description

Clinical Research Associate supporting sponsor-dedicated clinical trials across multiple U.S. locations. Responsibilities include site monitoring, protocol training, recruitment tracking, data quality oversight, and regulatory documentation management to ensure protocol compliance and data integrity.

Responsibilities

• Conduct site monitoring visits including initiation, ongoing monitoring, and closeout activities per protocol
• Partner with sites on subject recruitment planning and tracking to meet enrollment targets
• Deliver protocol training to sites and maintain regular communication on project expectations
• Assess study site quality and regulatory adherence; escalate compliance issues appropriately
• Track study progress including regulatory submissions, enrollment, CRF completion, and data queries

Requirements

• Bachelor's degree in scientific or healthcare discipline preferred
• Minimum 1.5 years of on-site clinical trial monitoring experience
• Knowledge of GCP and ICH guidelines for clinical research
• Proficiency with Microsoft Office (Word, Excel, PowerPoint)
• Strong written and verbal English communication skills
• Organizational, problem-solving, and time management abilities
• Ability to build effective working relationships with sites and team members

Compensation: $87,200 - $182,000 base

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