Principal Regulatory Writer
3 weeks ago
Join our esteemed organization as a Principal Regulatory Writer, where you'll be responsible for preparing high-quality clinical regulatory documents that comply with regulatory requirements.
About the Role:You will:
- Develop and execute comprehensive plans for document production, ensuring timely completion and meeting budget objectives.
- Liaise with clients to understand their needs, provide expertise on document content, and facilitate seamless communication among team members.
- Ensure consistency in document style, formatting, and content across all projects.
- Stay current with evolving regulatory landscapes and industry developments, applying this knowledge to enhance document quality and compliance.
- Minimum 3 years of experience in regulatory writing, with a strong focus on clinical documents.
- Experience in leading cross-functional teams and collaborating with clients to deliver high-quality documents.
- Degree in science/pharmacy (Postgraduate qualifications advantageous).
- Outstanding written and verbal communication skills.
- Ability to juggle multiple projects, meet deadlines, and adapt to changing priorities.
$130,000 - $160,000 per annum.
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