At a Glance
- Tasks: Lead inspection readiness and ensure regulatory compliance across clinical trials.
- Company: Join IQVIA LLC, a leader in healthcare data and analytics.
- Benefits: Competitive salary, travel opportunities, and professional development.
- Other info: Dynamic global environment with opportunities for career advancement.
- Why this job: Make a significant impact on clinical trial quality and compliance.
- Qualifications: Extensive GCP expertise and strong stakeholder engagement skills.
The predicted salary is between 80000 - 100000 £ per year.
IQVIA LLC is seeking a Clinical FSP Director Quality to lead inspection readiness and regulatory compliance across clinical trials.
You will drive proactive risk management, coordinate audit responses, and guide clinical teams on inspection expectations while maintaining continuous readiness.
The role requires extensive GCP expertise, regulatory knowledge, and senior stakeholder engagement across a matrix global environment, with travel as needed.
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EMEA Clinical Compliance & Inspection Director employer: IQVIA LLC
IQVIA LLC is an exceptional employer located in the vibrant town of Livingston, Scotland, offering a dynamic work culture that prioritises scientific excellence and patient outcomes. Employees benefit from comprehensive training and development opportunities, fostering personal and professional growth within the clinical lab services sector. With a strong emphasis on teamwork and innovation, IQVIA provides a rewarding environment for those looking to make a meaningful impact in healthcare.
