Senior Clinical Research Associate

Senior Clinical Research Associate role at ICON in the Northeast, focused on clinical trial monitoring and study operations. The position involves coordinating study setup, managing sponsor queries, maintaining documentation, and ensuring regulatory compliance within a sponsor-dedicated model.

Responsibilities

• Coordinate study setup and monitoring activities independently with accurate reporting
• Execute sponsor-generated queries and manage study cost efficiency
• Develop and maintain collaborative relationships with investigators and site staff
• Review study documentation and participate in feasibility assessments for new proposals
• Ensure patient safety and compliance with protocols and regulatory requirements

Requirements

• University degree in medicine, science, or equivalent field
• Knowledge of ICH-GCP guidelines and ability to review medical data
• Excellent written and verbal English communication skills
• Strong interpersonal skills for timely query resolution
• Willingness to travel approximately 60% as required

Compensation: $110,520–$138,150 base