We’re currently collaborating with a global, award-winning medical communications agency to support their search for an experienced Senior Regulatory Medical Writer. This is a unique opportunity to join a high-performing regulatory writing team, with exposure to international projects, complex document types, and strategic input in client programs. About the Role: As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. You’ll act as a primary point of contact for clients, support junior writers, and provide critical input on project strategy and delivery — all while working in a collaborative and supportive environment. This role is ideal for a confident communicator and experienced writer who thrives on ownership, autonomy, and the opportunity to mentor others. Key Responsibilities: Independently produce a range of high-quality regulatory documents (e.g., CSRs, protocols, IBs, CTD summaries, narratives) Critically review and provide strategic input into client documentation Act as a lead writer across multiple projects, overseeing timelines, quality, and team resourcing Coach and mentor junior writers, contributing to team knowledge sharing and best practice Serve as the expert point of contact for both internal stakeholders and external clients Participate in client meetings and proactively address issues and risks Ensure compliance with SOPs, industry regulations, and document standards Ideal Candidate Profile: Minimum of 5 years' regulatory writing experience in a medical communications agency or pharma/biotech setting Proven experience as lead writer across at least 3 document types (e.g., protocols, CSRs, IBs, Module 2.7 documents) BSc or PhD in life sciences (PhD preferred) Strong understanding of ICH and regulatory authority requirements Experience managing client relationships and project timelines Comfortable mentoring junior writers and delegating tasks effectively Ability to work independently and lead document strategy discussions Exceptional written and verbal communication skills What’s on Offer: Work with a global client base across therapeutic areas Highly supportive team culture and leadership Flexible/hybrid working options Strong focus on professional development and mentoring Opportunities for strategic project involvement and business development exposure Career progression pathways within a growing team