IQVIA in the UK is seeking an experienced Clinical Research Associate to monitor sites, ensure GCP compliance and data integrity across multiple protocols.
You will perform site visits, coordinate training, manage communications with study sites, and support regulatory submissions while traveling to assigned sites as needed. A life science degree and hands-on monitoring experience are required.
#J-18808-LjbffrClinical Research Associate — Onsite Monitoring & Trials in Reading employer: Meeveem Limited
Meeveem Limited is an exceptional employer that values its employees by fostering a collaborative and innovative work culture in the heart of Yorkshire. With a strong focus on professional development, employees are encouraged to grow their skills and advance their careers while enjoying competitive benefits and a supportive environment that prioritises work-life balance. Joining Meeveem means being part of a dynamic team dedicated to making a meaningful impact in the cardiovascular and endovascular sectors.
