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Principal Digital Process Lead
1 week ago
Serve as a Senior Clinical Quality Specialist, contributing to the success of our R&D Clinical Quality team. This role requires a deep understanding of GCP and regulatory requirements, as well as experience in verifying and approving SOPs.
Your primary responsibility will be to ensure regulatory compliance when transforming SOPs into digital/system-based processes. You will work closely with cross-functional teams and stakeholders to achieve this goal.
The ideal candidate will possess a master's degree in a relevant field, with at least 12 years of experience in clinical research and drug development. Strong English language skills and experience with digitalization of processes are also essential.
As a member of our hybrid team, you will enjoy a dynamic and flexible work environment. We offer opportunities for professional growth and development, and expect you to take ownership of your work and contribute to the success of our organization.
