At a Glance
- Tasks: Monitor clinical sites, ensure compliance, and support trial recruitment and documentation.
- Company: Join IQVIA, a leader in clinical research with a focus on innovation.
- Benefits: Competitive salary, travel opportunities, and professional development in a dynamic field.
- Other info: Exciting opportunities for growth in a fast-paced environment.
- Why this job: Make a difference in healthcare by supporting vital clinical trials and working with diverse teams.
- Qualifications: Strong communication skills and a passion for clinical research are essential.
The predicted salary is between 40000 - 50000 £ per year.
IQVIA UK’s Site Management team is expanding, seeking junior and experienced Clinical Research Associates to monitor sites across multi-sponsor studies, ensuring compliance with GCP/ICH and trial protocols.
You will work with sites to drive recruitment, train staff, manage documentation such as TMF/ISF, and collaborate with the study team to keep trials on track and within regulatory requirements.
Travel to sites is required, and strong communication with investigators is essential.
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Clinical Research Associate - Multi-Sponsor Site Monitoring in Ledston 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.
