Jobs at Parexel
Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Senior Regulatory Affairs Consultant
Job ID R0000037323 , BrazilThe 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.
Key Accountabilities:
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.
Skills:
High-level consulting skills.
Critical thinking and problem-solving skills.
Project leadership and management knowledge.
Excellent interpersonal and intercultural communication skills, both written and verbal.
Client-focused approach to work.
Results orientation.
Teamwork and collaboration skills.
Proficiency in local language and extensive working knowledge of the English language.
Networking.
Business analysis.
Self-confidence and control.
Education:
Minimum of a bachelor’s degree in a Scientific or Technical Discipline, Advanced Degree preferred.
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