Posted on 25th December 2025
Expires on 23rd February 2026
Negotiable
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
The Senior Consultant is responsible for overseeing end-to-end labeling development and implementation across Foundational markets (US, EU, CH, DE, AU) and non-US/Central EU regions. This role ensures compliance with country-specific regulatory requirements and manages operational processes for artwork creation, translation, and implementation. Acting as a key partner to Global Regulatory Affairs (GRA) Regions, Regulatory CMC, and Supply Chain, the Senior Consultant provides strategic guidance and operational leadership to support global labeling initiatives.
Oversees end-to-end labeling development and implementation for Foundational (US, EU, CH, DE, AU) and non-US/Central EU markets.
Key Responsibilities:
Ensure compliance with country-specific regulatory requirements.
Manage operational processes for artwork creation, translation, and implementation.
Act as key partner to GRA Regions, Regulatory CMC, and supply chain.
Critical thinking and problem-solving skills.
Project leadership and management knowledge.
Excellent interpersonal and intercultural communication skills, both written and verbal.
Proficiency in local language and extensive working knowledge of the English language.
Minimum of a bachelor’s degree in a Scientific or Technical Discipline, Advanced Degree preferred.