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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 Associate - Advertising & Promotional Labeling (home or office based)
Job ID R0000038654 , United KingdomAbout the Role
We are seeking an experienced Regulatory Affairs Associate or Senior Regulatory Affairs Associate to join our team! In this role you will be ensuring compliance with Health Authority drug promotion and promotional labeling regulations for assigned licensed products across Europe. This role combines deep regulatory expertise with consulting excellence to deliver high-quality services to our clients while advancing commercial success. You will review, approve, or reject promotional programming based on European regulations and guidance, ensuring adherence to established processes, SOPs, and work instructions.
Working within Parexel's consulting framework, you will provide regulatory leadership while delivering projects that meet both client and Parexel quality expectations. The role can be full remote or office based.
Key Responsibilities
Review advertising and promotional labeling materials; comment, improve, approve, or reject content based on company practice, policy, European law, and Health Authority regulations
Collaborate with Commercial Operations Marketing, Legal, and Medical personnel to minimize/mitigate Health Authorities enforcement risk while advancing commercial objectives
Monitor and apply trends in regulation of advertising and promotional labeling to review practices and processes
Provide regulatory leadership and guidance to marketing teams during development, review, and approval of promotional materials for assigned therapeutic areas
Prepare and submit advertising and promotional labeling materials to Health Authorities as required
Serve as Project Lead for small-scale projects or Work Stream Lead on larger projects
Skills and Experience required for the role:
University in a Scientific or Technical Discipline
Initial years in Regulatory Affairs relevant industry experience in Advertising & Promotional Labeling (required)
Ability to implement regulatory science and monitor enforcement trends
Capability to read and comprehend product-related technical and medical information
Client-focused approach with results orientation
Excellent teamwork and collaboration skills
Strong consulting skills with critical thinking and problem-solving abilities
Proficiency in English written and spoken
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