At a Glance
- Tasks: Oversee site monitoring and management for clinical research studies.
- Company: Join IQVIA LLC, a leader in healthcare data and analytics.
- Benefits: Competitive salary, professional development, and a supportive team environment.
- Other info: Exciting opportunity for career growth in a dynamic industry.
- Why this job: Make a difference in healthcare by ensuring quality in clinical trials.
- Qualifications: 2+ years of on-site monitoring experience and strong communication skills.
The predicted salary is between 31500 - 38500 £ per year.
IQVIA LLC is seeking a Clinical Research Monitor to oversee site monitoring and management, ensuring studies are conducted per protocol and regulatory requirements.
You will perform site visits, support data reporting, and work closely with study teams to maintain quality and timelines.
The role requires at least 2 years of on-site monitoring experience, strong communication and organizational skills, and proficiency with MS Office.
Visa sponsorship is not available for this position.
Senior Clinical Research Site Monitor in England employer: QPL IQVIA RDS Poland Sp. z o.o.
IQVIA is an exceptional employer that fosters a collaborative and innovative work culture, where your contributions directly impact global health outcomes. With a strong emphasis on employee growth, you will have access to mentorship opportunities and professional development resources, all while working in a dynamic environment that values diversity and creativity. Located in a vibrant area, our team enjoys a supportive atmosphere that encourages meaningful work and personal fulfilment.
Contact Details:
QPL IQVIA RDS Poland Sp. z o.o. Recruitment Team
