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Senior Regulatory Affairs Consultant - Labeling (US and Global Strategy Expertise)
Primary Location: United States, Remote Additional Locations: Canada, Quebec, Remote Job ID R0000036653 Category Regulatory Affairs Date Posted 11/19/2025Overview
As part of Parexel Consulting, you will play a vital role in helping biopharmaceutical and medical device companies navigate the complex and ever-changing regulatory landscape. Drawing on your scientific, technical, and regulatory expertise, you will work closely with clients to develop and implement regulatory strategies that bring their products to market faster and keep them there.
We value collaboration, innovation, and continuous learning. As a member of our team, you will partner with a diverse group of clients, and be exposed to various product types and therapeutic areas. You will also develop your skills through challenging assignments and mentorship from experienced regulatory professionals. Plus, you will enjoy the flexibility of working remotely while still being part of a supportive and dynamic team.
Success Profile
Do you have these soft skills and interpersonal traits to succeed at Parexel?
- Communicator
- Detail-oriented
- Problem-solver
- Relationship-builder
- Results-driven
- Strategic
About This Role
Incredible, high-impact role with a Global Biopharma sponsor!
Are you ready to turn your labeling expertise into strategic impact?
We’re seeking a sharp, detail-driven Senior/Consultant, Regulatory Labeling to join a dedicated partnership with a leading global biopharmaceutical company. In this high-visibility role, you’ll be more than a consultant — you’ll be a trusted collaborator whose insights help shape regulatory strategy and ensure patients worldwide receive safe, effective therapies with clarity and confidence
In this role, you’ll be the go-to expert for global labeling, working side-by-side with client teams across Regulatory Affairs, Technical Operations, Safety, and Commercial. You’ll help navigate the complex regulatory landscape, ensure compliance across international markets, and drive continuous improvement in how labeling is developed, tracked, and delivered.
Key Responsibilities:
• Serve as the global labelling lead for multiple products, providing strategic direction and oversight.
• Lead the development and maintenance of Company Core Data Sheets (CCDS), local labels, and associated labelling components.
• Chair the Cross-Functional Labelling Team (XLT), facilitating the development of label updates and enabling senior management review and approval.
• Ensure regional labelling compliance with CCDS standards.
• Evaluate health authority comments for labelling implications and lead the development of appropriate responses.
• Participate in Safety Management Team (SMT) and Global Regulatory Team (GRT) meetings to provide expert input on labelling matters.
• Monitor emerging safety signals and assess potential impact on labelling.
• Provide strategic insight and guidance on labelling topics to support regulatory and safety objectives.
This role is ideal for a candidate with a strong background in regulatory affairs, labelling strategy, and cross-functional leadership. It offers the opportunity to make a meaningful impact on global product communication and patient safety.
Additional Responsibilities:
As a Senior Consultant/Consultant, Regulatory Labeling, you will partner with Label Strategist to:
Conduct international labeling operations activities to support global new product and supplemental applications to product registration, and post approval launches for impacted international markets.
Collaborate with Technical Operations team members to ensure commercial distribution, Regulatory Technology for labeling submissions, PV for safety reporting, and other functional groups. Provide labeling to Advertising and Promotion for marketing pieces, and with Commercial for website postings if needed.
Work with Regulatory Operations, Regulatory Affairs, Tech Ops, etc. for labeling distribution, tracking and quality control.
Utilize regulatory/product knowledge to provide operational support to ensure that labeling materials meet regulatory and company requirements and timelines.
You will also:
Be responsible for executing and effective quality control reviews and tracking (primarily) internally used labeling documents (Core Data Sheet, Core Patient Information Leaflet, Core Instructions for Use) and outward facing local/regional labeling (USPI, Med Guide, SmPC, PIL, Canadian Product Monograph, Instructions for Use) as well as container and carton labels to meet regional regulatory requirements and ensure consistency between labeling, labels and supportive documents.
Act as operational expert for Global Labeling tracking in RIMs, SPL generation, ensure development and maintenance of templates, collaboration features and system upgrades.
Contribute to the continuous improvement of the end-to-end labeling process including excellent proofreading/editing skills and compiling supportive documentation.
Support labeling inspection / audit readiness activities
Education and Experience
Bachelor’s Degree plus at least 4+ years of experience in drug development especially in labeling, product package coordination, clinical supplies/packaging, supply chain regulatory affairs, or quality. Exceptional candidates with 3+ years of labeling related experience may also be considered
Good working knowledge of key labeling regulations/guidance and past experience in label development (CCDS, USPI, packaging)
The ability to research and create comparator labeling documents
Strong understanding and past experience creating annual reports
The ability to collaborate with Tech Ops for artwork implementation
Proficiency in SPL (all aspects, types and troubleshooting) and the ability to manage the review and approval of labeling in a document management system.
Electronic document management systems use and / or electronic submission experience
Knowledge and Skills
Strong attention to detail
Solid understanding and interpretation of US labeling regulatory requirements preferred
Solid understanding of requirements for tracking of labeling updates
Solid understanding of the pharmaceutical industry drug development process and willingness to learn global labeling regulatory requirements and industry practice
Solid aptitude for use of IT systems; Regulatory Information Management System (RIMS), electronic document management system (EDMS), Proficiency in MS Office suite; Willing to learn additional applications
Understanding of label development and submission processes preferred.
Ability to recognize and escalate issues
Strong written and oral communication and organizational skills
Ability to generate and initiate problem solving innovative solutions
The ideal candidate should be action-oriented, customer focused, ability to manage workloads and set priorities. In addition, he/she should be capable of dealing with ambiguity, be creative, and be comfortable working with multifunctional teams
If you thrive in fast-paced, high-stakes environments and love the idea of being a key player in a global regulatory role - apply today!
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EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the United States includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
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