Senior Clinical Research Associate

This role involves overseeing clinical trial monitoring activities for Phase I oncology studies across New York and New Jersey sites. The Senior CRA will manage site compliance with protocols and regulatory standards, conduct site visits, mentor staff, and coordinate cross-functional teams to ensure data integrity and trial execution. Requires a bachelor's degree in a scientific field, extensive clinical research experience, and willingness to travel approximately 60% of the time.

Responsibilities

• Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standards
• Conduct site visits to assess performance, troubleshoot issues, and provide operational support
• Collaborate with cross-functional teams on accurate data collection and reporting
• Train site staff and other CRAs to maintain high standards of trial conduct
• Build and maintain relationships with site personnel to support trial operations

Requirements

• Bachelor's degree in scientific or healthcare-related discipline
• Extensive clinical research associate experience with knowledge of trial processes
• Ability to manage multiple sites and projects with strong organizational skills
• Expertise in monitoring practices, data integrity, and site management
• Proficiency in clinical trial software and relevant tools
• Excellent communication and stakeholder management abilities
• Willingness to travel approximately 60% of the time

Compensation: $110,520-$138,150 base