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.

• 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 submissions
• Proven experience in regulatory or technical scientific writing
• Strong communication, interpersonal, and project management skills
• Proficiency with document management systems and standard software tools