At a Glance
- Tasks: Monitor clinical trials and ensure compliance with protocols and guidelines.
- Company: Join IQVIA UK, a leader in healthcare data and analytics.
- Benefits: Attractive salary, career development, and a supportive team environment.
- Other info: Exciting opportunity for growth in a dynamic and innovative company.
- Why this job: Make a difference in healthcare by ensuring successful trial management.
- Qualifications: Experience in clinical research and strong organisational skills.
The predicted salary is between 30000 - 40000 £ per year.
IQVIA UK is expanding its Site Management team and is hiring two Senior CRAs.
You will perform monitoring and site management activities to ensure trials run in compliance with the protocol, GCP, ICH guidelines, and sponsor requirements.
You will visit sites for initiation, monitoring and close-out visits, support subject recruitment plans, train site staff, track regulatory submissions, and maintain documentation in the TMF/ISF.
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Senior CRA: On-site Monitoring & Site Management 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.
