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Role: Senior / Principal Regulatory WriterBusiness Unit: Bioscript Regulatory WritingLocation: UK (Hybrid or UK remote) About UsEstablished in 2005, Bioscript Group is formed from multiple, specialist businesses to support our global pharmaceutical clients; we provide multidisciplinary expertise to help our clients navigate critical decisions at key points in the product lifecycle. ​Our scientific and strategic expertise help our clients make better decisions. We provide medical communication services, market access consulting and regulatory writing support with deep domain expertise to effectively navigate complex disease areas.The OpportunityWe are hiring for both Senior Regulatory Writer (SRW) and Principal Regulatory Writer (PRW) positions. This is a fantastic opportunity to join our friendly and supportive team and lead the development of high-quality regulatory documents. You will work closely with our clients and internal teams, providing technical and scientific leadership, and ensuring the delivery of clear, accurate, well-written documents.Key Responsibilities (SRW and PRW)Lead and motivate regulatory writing team members, adhering to company policies and procedures. Coach and mentor more junior team members, providing support and guidance on client and project-related issuesBe the point of contact for specific project deliverables, managing the technical and scientific aspects of leadership of designated client accounts/teamsTake responsibility for the delivery of multiple projects across client accounts, ensuring high-quality work that meets the project/client brief, timelines, and budget Track and manage project scope in collaboration with the Project Management team, demonstrating a sound understanding of budgets Proactively share knowledge and experience to support the transfer of knowledge across the team Support development of the regulatory writing training programme, as appropriateLine management, if consistent with company needs and personal aspirationsAdditional PRW ResponsibilitiesLead strategic and high-complexity programs such as submissionsBe a key source of account, product, or therapy area expertise to clients and colleaguesAdvise on regulatory writing processes and strategy, document quality process, client procedures, and best practice for projectsContribute to group discussions, sharing opinions and professional valuesSupport the Project Management team with development or review of budgets against project specifications, if requiredContribute to ongoing recruitment programmes, assisting with candidate assessment and the interview process, if requiredAbout YouStrong technical and scientific skills with experience in developing high-quality regulatory documents Excellent communication skills and the ability to coach and mentor junior team members, providing support and guidance on client and project-related issuesAbility to manage multiple projects and deliver high-quality work within deadlines, ensuring the production of clear, accurate, and grammatically correct written workA proactive approach to sharing knowledge and supporting team development, contributing to the transfer of knowledge across the teamOur people are at the heart of our businessWe are focused on delivering the exceptional, not just for our clients, but for our teams too. We treat everyone as individuals and provide opportunities to develop your skills and career around our disciplines.Our benefits include: Salary which aligns with your experience and skillset 25 days holiday + bank holidays + winter shutdown + holiday purchase schemeEnhanced sick and compassionate leave Enhanced maternity, paternity and adoption leaveBirthday donation to a charity of your choice Bonus day off to be spent giving back to the communityLife Insurance and Critical Illness cover Private Medical Insurance (Vitality for UK based colleagues)Health cash plan or wellbeing allowanceInternational Employee Assistance Program