At a Glance
- Tasks: Conduct monitoring visits and ensure data integrity for clinical trials.
- Company: CCS-Global, a leader in quality-centric site management.
- Benefits: Hybrid working model, comprehensive training, and stability with single-sponsor teams.
- Other info: Join a supportive team with opportunities for growth in the healthcare sector.
- Why this job: Make a real difference in clinical research while developing your skills.
- Qualifications: Relevant monitoring experience and understanding of ICH-GCP guidelines.
The predicted salary is between 30000 - 40000 £ per year.
CCS-Global is hiring Clinical Research Associates I & II in the United Kingdom, focusing on quality site management. Candidates should have relevant monitoring experience and a strong understanding of ICH-GCP guidelines.
The position offers a hybrid model of working with dedicated single-sponsor teams, providing stability and comprehensive training.
The role includes:
- Conducting monitoring visits
- Ensuring data integrity
- Acting as the primary contact between sponsors and investigative sites
Home-Based CRA I/II – Quality-Centric Site Monitoring in London employer: CCS-Global
CCS-Global is an exceptional employer, offering Clinical Research Associates a unique opportunity to thrive in a supportive and quality-focused environment. With a hybrid working model and dedicated single-sponsor teams, employees benefit from stability, comprehensive training, and a culture that prioritises professional growth and collaboration. Join us to make a meaningful impact in clinical research while enjoying a rewarding work-life balance.
