At a Glance
- Tasks: Monitor clinical studies on-site and ensure compliance with regulations.
- Company: Join IQVIA, a leader in clinical research and innovation.
- Benefits: Full-time role with career development opportunities and competitive salary.
- Other info: Build strong relationships in a dynamic and supportive environment.
- Why this job: Make a difference in healthcare by ensuring quality in clinical trials.
- Qualifications: 2+ years of monitoring experience and a relevant scientific degree.
The predicted salary is between 30000 - 40000 £ per year.
IQVIA Argentina is seeking a dedicated professional for an on-site monitoring role in Reading, United Kingdom. The position requires at least 2 years of experience in monitoring interventional studies, ensuring compliance with regulatory requirements including Good Clinical Practice (GCP).
The ideal candidate will have a degree in a relevant scientific discipline and be adept at building effective working relationships. This is a full-time field-based role offering career development opportunities.
Clinical Research Associate II: Site Monitoring in Reading employer: IQVIA Argentina
At IQVIA, we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. Our Reading location offers a hybrid working model, allowing for flexibility while engaging in meaningful projects that impact clinical outcomes globally. We are committed to employee growth, providing ample opportunities for professional development and mentorship, making it an ideal place for those looking to advance their careers in clinical research.
