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. We are seeking a Senior Regulatory Affairs Associate to join a dedicated client project supporting the implementation of approved labelling content into compliant packaging and artwork materials for pharmaceutical products. You will work closely with Regulatory Affairs, Labelling Operations, Artwork Management and Change Control teams to coordinate the accurate and timely creation, review and progression of package leaflets, cartons, labels and related packaging components. You will be the key liaison between regulatory, operational, graphics and artwork teams throughout the artwork lifecycle, with the experience to take ownership of workstreams and support more junior colleagues. This role can be home or office based in various European locations. Role responsibilities: Artwork and packaging coordination Coordinate the progression of approved labelling content through artwork development, review, approval and implementation. Support the creation and maintenance of package leaflets (PILs), cartons, labels, foils, booklets and other packaging components. Ensure approved regulatory content is accurately transferred into artwork and packaging assets. Track artwork activities and monitor delivery against agreed timelines, priorities and client requirements. Cross-functional collaboration Coordinate with EU and US labelling leads to implement approved labelling changes. Partner with local regulatory teams and artwork or change-control teams to facilitate market-specific updates. Act as a central point of contact between Regulatory Affairs, Labelling Operations, artwork production, graphics and other stakeholders. Escalate risks, delays, discrepancies and unclear requirements to the appropriate stakeholders for resolution. Change control and compliance Lead change-control activities associated with labelling and packaging updates. Maintain documentation, records and approval evidence throughout the artwork process. Perform all activities in accordance with applicable regulatory requirements, internal procedures and quality standards. Lead investigation and resolution of artwork-related issues, content discrepancies and implementation questions. Documentation, translations and systems Maintain accurate status information for artwork activities, approvals and implementation milestones. Use document management, artwork management and workflow systems in line with established procedures. Coordinate translations and multilingual artwork requirements, including follow-up on queries and approvals. Contribute to process improvement and consistency across labelling and artwork operations. Provide guidance and training to junior team members as required. Skills and Experience required for the role: University degree in life sciences discipline. Experience in pharmaceuticals, biotechnology, consumer health, healthcare or another regulated industry. Experience or knowledge of artwork management, change control, translations, graphics, regulatory labelling, packaging or technical documentation. Strong organisational skills, attention to detail and the ability to manage multiple activities and priorities. Clear written and verbal communication skills, with the ability to work effectively across functions and regions. Ability to follow controlled processes, maintain accurate records and identify inconsistencies. Proficiency in electronic workflow and document-management systems. Fluent in English, written and spoken. Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our professionals worldwide work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind — broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40+ years and drives us forward, advancing clinical research in healthcare’s most complex areas while harnessing innovation to drive efficiencies across every phase of the clinical development process. Our insights-driven approach, proven delivery and trusted execution are accelerating the delivery of life-changing treatments to patients — With Heart.™

Senior Regulatory Affairs Associate - Artwork Coordinator (home or office based).

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