IQVIA LLC is seeking an on-site monitoring professional to ensure adherence to GCP and protocol requirements across multiple sites. You will manage site communications, training, and issue resolution while tracking regulatory submissions and data queries throughout the study lifecycle.
The role requires at least 1 year of on-site monitoring experience, strong knowledge of GCP/ICH guidelines, and proficiency in Word/Excel/PowerPoint.
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Clinical Research Associate II – Onsite Monitoring in Langley employer: IQVIA LLC
At IQVIA, we pride ourselves on being an exceptional employer, particularly for those in the field of Pharmaceutical Development. Our Cambridge location fosters a collaborative and innovative work culture, where you will have the opportunity to influence scientific direction, mentor junior scientists, and engage directly with clients. With a strong focus on employee growth and the integration of cutting-edge AI-enabled approaches, we are committed to supporting your professional development while making a meaningful impact in the pharmaceutical industry.
