Job Description

Clinical Research Associate position focused on sponsor-dedicated monitoring and site management for clinical trials. Responsible for conducting site visits, managing recruitment, ensuring protocol compliance, and maintaining regulatory documentation across multiple study sites.

Responsibilities

• Conduct site monitoring visits including initiation, ongoing monitoring, and closeout activities
• Develop and track subject recruitment plans with study sites to meet enrollment targets
• Provide protocol training and maintain communication with assigned sites
• Evaluate study site compliance with protocol requirements and applicable regulations
• Track study progress including regulatory submissions, enrollment metrics, 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 Good Clinical Practice and ICH guidelines
• Proficiency with Microsoft Office Suite and standard computer platforms
• Strong written and verbal English communication skills
• Organizational and problem-solving abilities
• Ability to build effective working relationships with diverse stakeholders

Compensation: $90,200–$190,000 base

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