Clinical Research Associate: Site Monitoring & Study Oversight

Clinical Research Associate: Site Monitoring & Study Oversight

Full-Time No working from home possible
IQVIA

IQVIA UK’s Site Management (multi-sponsor) team is growing and seeking junior and experienced Clinical Research Associates.

You will perform site monitoring visits, drive subject recruitment plans, train site staff on the protocol, and maintain open lines of communication to manage expectations, with a focus on quality and data integrity.

This role requires GCP/ICH knowledge, the ability to travel, and a commitment to regulatory compliance across diverse sites.

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Clinical Research Associate: Site Monitoring & Study Oversight employer: IQVIA

IQVIA in Livingston, Scotland is an excellent employer that fosters a collaborative team environment and prioritises employee growth through outstanding career development opportunities. Working as a Lab Operations Assistant here not only allows you to contribute to meaningful projects but also ensures you are part of a supportive workplace that values safety and professionalism.

IQVIA

Contact Details:

IQVIA Recruitment Team