Clinical Content Specialist
3 weeks ago
We are Vivify Talent Limited, a specialty pharmaceutical company that is passionate about innovation and excellence. As a Principal Regulatory Writer, you will be responsible for creating high-quality clinical documents that meet regulatory requirements. This role can be home-based anywhere.
In this role, you will work closely with our clinical and regulatory teams to develop documents that showcase our expertise in the field of pharmaceuticals. You will have the opportunity to work on a broad range of clinical documents, from protocols to reports. Your goal will be to ensure that all documents are accurate, clear, and compliant with regulatory guidelines.
Key Responsibilities:
- Develop high-quality clinical documents, including protocols, reports, and other regulatory submissions.
- Collaborate with cross-functional teams to ensure that documents meet regulatory requirements and are aligned with business goals.
- Conduct research to stay up-to-date with the latest regulatory developments and guidelines.
- Identify areas for improvement and implement changes to enhance document quality and efficiency.
Requirements:
- Bachelor's degree in a life science or related field.
- Minimum 5 years of experience in clinical writing or a related field.
- Proven track record of developing high-quality clinical documents that meet regulatory requirements.
- Strong understanding of regulatory guidelines and industry standards.
- Excellent communication and collaboration skills.
Benefits:
- Competitive salary: $110,000 per year.
- Flexible work arrangements, including remote work options.
- Opportunities for professional growth and development.
- Collaborative and dynamic work environment.
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