Regulatory Scientific Writer Role
Our client, a global pharma company, is currently seeking a skilled Scientific Writer Regulatory to join their team. As a key member of the Global Scientific Communications team, you will be responsible for creating high-quality regulatory documents that ensure 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.
Requirements include a Bachelor's degree in life sciences, health, communications, or related field, as well as expertise in relevant therapeutic areas and experience with clinical development and regulatory submissions. Strong communication, interpersonal, and project management skills are essential for success in this role.