At a Glance
- Tasks: Monitor clinical sites and ensure compliance with study protocols and regulations.
- Company: Join a leading global healthcare company dedicated to improving patient outcomes.
- Benefits: Attractive salary, flexible working options, and opportunities for professional growth.
- Other info: Be part of a dynamic team with a focus on innovation and collaboration.
- Why this job: Make a difference in healthcare by ensuring studies run smoothly and effectively.
- Qualifications: Experience in clinical research and strong organisational skills required.
The predicted salary is between 40000 - 50000 £ per year.
IQVIA UK is seeking two Senior CRAs to join the Site Management team in Reading.
You will perform on-site monitoring to ensure sites conduct the study according to protocol, GCP, ICH, and sponsor requirements, while supporting recruitment plans and study documentation.
You will manage regulatory submissions, CRF completion, and data queries, collaborating with the study team to drive project success and maintain TMF/ISF records.
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Senior CRA I: Site Monitoring & Study Leadership in Reading 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.
