Associate Director: Quality Process & Documentation

IQVIA is seeking an Associate Director Quality – Client Dedicated Process & QD Manager in Basel to oversee quality documentation and training management. The role requires deep expertise in clinical development with a minimum of 12 years of experience in the pharmaceutical industry.

The associate director will ensure compliance with documentation standards, coordinate audits, and lead training programs. Excellent organizational and interpersonal skills are necessary for effective collaboration across virtual international teams.