Job Description

Senior Clinical Research Associate in Boston overseeing clinical trial monitoring and site management at a large contract research organization. Role focuses on ensuring protocol adherence, regulatory compliance, and quality standards across multiple trial sites while leading and mentoring junior staff.

Responsibilities

• Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standard maintenance
• Conduct site visits to evaluate performance, troubleshoot issues, and provide operational support
• Collaborate with cross-functional teams on accurate and timely data collection and reporting
• Train and mentor site staff and CRAs on clinical trial best practices and standards
• Establish and maintain relationships with site personnel to support trial execution

Requirements

• Bachelor's degree in scientific or healthcare-related field
• Extensive experience as Clinical Research Associate with deep trial process knowledge
• Ability to manage multiple sites and projects concurrently with strong organizational skills
• Expertise in monitoring practices, data integrity, and clinical trial software systems
• Excellent communication and stakeholder management abilities
• Willingness to travel approximately 60% as required

Compensation: $110,520–$138,150 base

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