This a Full Remote job, the offer is available from: Hungary, Poland, Romania, Czechia, Croatia, Serbia, Oregon (USA) 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 an experienced Regulatory Affairs Consultant Safety & Labelling to develop and execute artwork strategies for our global product portfolio. In this critical role, you will ensure comprehensive oversight throughout the product lifecycle while serving as the primary liaison between Regulatory Affairs and various stakeholders. The role can be home or office based in various European locations. Role Responsibilities: • Conduct and deliver high quality, on time safety labelling regulatory activities, including compliant management of all internal tools and client systems; • Author administrative and regulatory documents/deliverables and collaborate with project SMEs and client stakeholders to prepare submission packages; • Full management of safety labelling submissions (i.e. planning, submission package compilation, RIMS maintenance, RtQ preparation, Spontaneous HA queries, etc.); • Act as main GRA point of contact for local regulatory and other stakeholders • Tracking and management of all EU Product Information, alignment with QRD requirements and ability to manage EU linguistic review, readability testing and translation activities. • Supporting regulatory inputs into Periodic Safety Update Reports (PSUR) and potential impact on labelling • Participation in change control process for safety labelling update Skills and Experience required for the role: • Bachelor's Degree in a Scientific or Technical Discipline • Knowledge of EU regulatory requirements for medicinal product labelling • Familiarity with the Company Core Datasheet (CCDS) and its implementation into labelling and artworks • Understanding of Safety Signal Management and the impact of confirmed safety signals on labelling • Excellent communication and stakeholder management skills; • Strong organizational and time management skills; • Strong problem-solving skills; • Coordinate all assigned activities; • ‘Proactive’ and ‘efficient' work ethic; • Strong oral and written communication skills, with proven ability to work efficiently as part of a team; • Strong interpersonal skills; • Fluent in English, written and spoken This offer from "Parexel" has been enriched by Jobgether.com and got a 86% flex score. Apply tot his job