At Parexel, we are committed to improving the world's health through our clinical development solutions. The Regulatory Affairs Consultant will manage the end-to-end labeling lifecycle and ensure compliance with local requirements. This role offers the flexibility to work fully home-based or office-based, contributing to a patient-focused mission
Job Summary
At Parexel, we are committed to improving the world's health through our clinical development solutions. The Regulatory Affairs Consultant will manage the end-to-end labeling lifecycle and ensure compliance with local requirements. This role offers the flexibility to work fully home-based or office-based, contributing to a patient-focused mission.
Matching Summary
At Parexel, we are committed to improving the world's health through our clinical development solutions. The Regulatory Affairs Consultant will manage the end-to-end labeling lifecycle and ensure compliance with local requirements. This role offers the flexibility to work fully home-based or office-based, contributing to a patient-focused mission.
Skills & Requirements
Must-have
Global labelling operations expertise
Experience with CCDS development
Attention to detail and organizational skills
Nice-to-have
Experience leading teams in a matrix organization
Ability to work in a global team environment
Fluent in German and English
Key Requirements
University degree in life science
A few years of experience in biotech/pharmaceutical
Labelling/regulatory experience with global responsibilities