Description
Join IQVIA on our mission to accelerate innovation for a healthier world!
IQVIA's Site Management (full service / multi-sponsor) team is growing and seeking experienced Clinical Research Associates.
Why IQVIA? We offer genuine career development opportunities, AI-powered career advancement through our internal talent marketplace, Career Connections, mentorship opportunities, flexible working, and well-being support.
Awards We have received several awards, including 2026 'Glassdoor Best Place to Work in the UK', #1 in category - 2026 Fortune World's Most Admired Companies list (for the fifth consecutive year!), and Brandon Hall Excellence Award for Learning & Development.
Responsibilities As a Clinical Research Associate, you will:
- Perform site monitoring visits in accordance with contracted scope of work and regulatory requirements
- Work with sites to adapt, drive, and track subject recruitment plans
- Administer protocol and related study training to assigned sites
- Evaluate the quality and integrity of study site practices
- Manage the progress of assigned studies
- Ensure copies of site documents are available for filing in the Trial Master File
- Create and maintain documentation regarding site management, monitoring visit findings, and action plans
- Collaborate with study team members for project execution support
Requirements To be successful in this role, you will need:
- At least 2 years of on-site monitoring experience of interventional studies
- A degree in a scientific discipline or healthcare, or equivalent industry experience
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements
- Ability to establish and maintain effective working relationships with coworkers and clients
Please note that this position is not eligible for visa sponsorship.
Apply today and forge a career with greater purpose, make an impact, and never stop learning!