IQVIA LLC is seeking a Clinical Research Monitor to oversee site monitoring and management, ensuring studies are conducted per protocol and regulatory requirements. You will perform site visits, support data reporting, and work closely with study teams to maintain quality and timelines.
The role requires at least 2 years of on-site monitoring experience, strong communication and organizational skills, and proficiency with MS Office. Visa sponsorship is not available for this position.
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Senior Clinical Research Site Monitor 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.
