Scientific Writer Regulatory Specialist
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We are seeking a skilled Scientific Writer to join our team on a permanent basis. The role involves creating high-quality regulatory documents, collaborating with cross-functional teams, and ensuring clear, accurate, and compliant scientific content throughout the drug development lifecycle.
Key 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.
Required Skills and Qualifications:
* 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.
Benefits:
This role offers hybrid working, allowing for flexibility and work-life balance.