At a Glance
- Tasks: Lead quality management activities and ensure compliance in clinical trials.
- Company: Join IQVIA, a leader in healthcare data and analytics.
- Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: Dynamic role with occasional travel and a collaborative team environment.
- Why this job: Make a difference in clinical research while working flexibly.
- Qualifications: Bachelor's degree and 4+ years of clinical research experience required.
The predicted salary is between 45000 - 60000 £ per year.
IQVIA LLC in Reading, Berkshire, is seeking a Sr Quality Specialist to implement the Global Quality Management Plan. You will execute quality management activities, conduct risk assessments, and support compliance with GCP and SOPs.
The ideal candidate should have a Bachelor's degree and a minimum of 4 years of clinical research experience, including monitoring experience.
This role offers a hybrid working model with expected office presence of 2-3 days per week and may require occasional travel.
Quality & Compliance Lead – Clinical Trials (Hybrid) employer: IQVIA LLC
IQVIA LLC is an exceptional employer that prioritises employee growth and development within the dynamic field of clinical trials. With a hybrid working model that promotes work-life balance, employees benefit from a collaborative culture that encourages innovation and compliance excellence. Located in Reading, Berkshire, team members enjoy access to a vibrant community while contributing to impactful healthcare solutions.
