Scientific Content Specialist
Há 5 dias
This is a challenging role that requires expertise in creating regulatory materials for pharmaceutical products.
The ideal candidate will have a strong background in scientific writing, with experience in creating documents such as protocols, CSRs, and briefing books.
- Serve as lead writer on regulatory documents.
- Manage timelines and communications for concurrent writing projects.
- Organize document review meetings and incorporate feedback from cross-functional teams.
Key Responsibilities:
- Craft clear and concise regulatory content.
- Collaborate with subject matter experts to resolve feedback and align messaging.
- Develop project-level lexicons and conventions.
Requirements:
- Advanced degree in a scientific discipline or relevant work experience.
- Mastery of 3 or more regulatory document types.
- Strong attention to detail and ability to apply regulatory guidelines.
Benefits:
- Flexible remote work arrangements.
- Ongoing training and development opportunities.
- A collaborative and dynamic work environment.
What We Offer:
- A competitive compensation package.
- A comprehensive benefits program.
- A chance to work on high-profile projects and make a real impact in the industry.
About Us:
- We are a leading provider of regulatory services to the pharmaceutical industry.
- We pride ourselves on our expertise and commitment to delivering high-quality results.
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