Teams at ICON plc

As a Senior Clinical Research Associate, you will design and analyze clinical trials, ensure protocol compliance, and maintain data integrity while collaborating with investigators. Traveling 60% of the time is required.

The Senior Clinical Research Associate will manage site activities and ensure compliance during Oncology clinical trials, focusing on data integrity and subject safety.

Oversee cardiovascular clinical trials, ensuring compliance with regulations while managing site relationships and communication. Requires 3 years of monitoring experience and strong problem-solving skills.