Scientific Writer

Scientific Writer Regulatory Our client, a global pharma company, are currently growing their Global Scientific Communications team and are currently seeking a skilled Scientific Writer Regulatory to join their team on a permanent basis. As Scientific Writer Regulatory you will be responsible for the creation of high-quality regulatory documents (e. g. , clinical study reports, briefing packages, regulatory responses, IND/MAA submissions). The role involves collaborating with cross-functional teams to ensure clear, accurate, and compliant scientific content throughout the drug development lifecycle. This role offers hybrid working. Responsibilities: Document Development:

Plan, write, edit, and finalize regulatory documents; ensure data accuracy, clarity, and consistency; coordinate reviews and incorporate feedback. Project Management: Develop timelines, manage risks, track progress, and maintain communication with stakeholders to deliver on schedule. Scientific Expertise: Maintain up-to-date knowledge of assigned therapeutic areas, compounds, and relevant regulatory guidelines. Collaboration & Coaching: Share best practices, provide guidance to colleagues, and contribute to process improvements. Requirements: Bachelor’s degree in life sciences, health, communications, or related field. Advanced degree with research background. Expertise in relevant therapeutic areas (e. g.

, oncology, neuroscience, immunology)Experience with clinical development and regulatory submissionsProven experience in regulatory or technical scientific writingStrong communication, interpersonal, and project management skillsProficiency with document management systems and standard software tools