IQVIA is seeking a Senior CRA to conduct site qualification, initiation, monitoring, and close-out visits in line with study protocols and regulatory standards. You will safeguard patient safety, data integrity, and protocol compliance while guiding investigators and site staff throughout the study lifecycle.
You will monitor regulatory documentation, recruitment, data queries, and site performance, collaborating with cross-functional teams to optimize recruitment and ensure timely delivery.
#J-18808-Ljbffr
Senior Clinical Research Associate — Global Monitoring Lead 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.
