
Senior Scientific Content Developer
17 hours ago
This role requires a skilled writer to prepare scientific publications, including abstracts, posters, manuscripts, presentations, and regulatory documents.
- Key responsibilities include document preparation, development, and finalization/document management.
- Evaluate data, information, and input from multiple sources, functions, and regions.
- Plan, write, edit, review, and coordinate the publication of scientific data in peer-reviewed journals and forums/regulatory documents supporting clinical development/product registration.
- Ensure key data, strategically aligned scientific narrative, elements from internal guidance and resource documents are included appropriately in all documents.
- Exhibit flexibility in moving across development and preparation of multiple document types.
- Work with teams to ensure smooth and timely development of documents and escalate issues, as appropriate, to ensure document completion.
The ideal candidate will have a Bachelor's degree in a scientific, health, communications, or technology-related field or equivalent experience in clinical development.
Requirements:
- Demonstrated experience of verbal and written English skills in the medical, scientific, or technical writing fields.
- Experience writing regulatory, clinical trial documents, and/or publications.
- Clinical pharmacology, therapeutic area, or other medical and scientific specific knowledge and experience specific to the hiring area.
About this Role:
- Foster collaboration and open communication among cross-functional teams.
- Broaden your knowledge and expertise in various scientific areas.
- Contribute to the development of high-quality scientific documents.
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