Senior Clinical Associate

ICON seeks a Clinical Associate to support the design, implementation, and management of clinical trials in a sponsor-dedicated model. The role involves coordinating study activities, maintaining documentation, and collaborating across cross-functional teams to ensure protocol adherence and data integrity.

Responsibilities

• Assist in planning, execution, and monitoring of clinical trials with protocol and regulatory adherence
• Coordinate site initiation, patient recruitment, data collection, and monitoring visits
• Collaborate with Clinical Operations, Data Management, and Biometrics teams
• Maintain comprehensive study documentation and records in compliance with regulations
• Support study close-out activities including data cleaning and report preparation

Requirements

• Bachelor's degree in relevant scientific or healthcare-related discipline
• Minimum 2 years clinical trial associate experience in pharmaceutical, biotechnology, or CRO
• Proficiency with Trial Master File (TMF) and clinical trial technologies
• Strong organizational and time management capabilities with ability to prioritize competing priorities
• Excellent attention to detail and data accuracy commitment
• Cross-functional collaboration and communication skills
• Willingness to travel approximately 60% as required