Associate Scientific Writer
Thermo Fisher Scientific
full-time
Posted on:
Location Type: Remote
Location: Virginia • United States
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About the role
- Prepares and/or assists in the coordination and preparation of scientific documents under direct supervision to meet or exceed quality standards.
- Writes and edits scientific documents such as analytical methods, method development summaries, reports, and protocols and ensures compliance with required formats and SOPs for potential submission to regulatory authorities.
- Compiles laboratory data into a specified report format.
- Reviews data tables and ensures that errors are corrected.
- Performs a quality control review of scientific documents prior to creation of the final PDF deliverable.
- Ensures compliance with PPD Laboratory Services, Client, and eCTD policy.
- Reviews scientific documents for accuracy, formatting, consistency, and compliance to protocols or SOPs.
- Keeps updated on the guidelines and requirements of the FDA and other international regulatory agencies for reference in the development of required documents.
Requirements
- Bachelor's degree, or equivalent experience.
- Exceptional command of written and spoken English.
- Strong attention to detail and ability to maintain scientific rigor.
- Proficiency in scientific software and databases.
- Experience in scientific writing strongly preferred.
- Knowledge of scientific terminology, medical, pharmaceutical, and research concepts.
Benefits
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Applicant Tracking System Keywords
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Hard Skills & Tools
scientific writingdata compilationquality control reviewregulatory complianceSOPsanalytical methodsmethod developmentreport writingdocument editingscientific terminology
Soft Skills
attention to detailcommunicationorganizational skillsscientific rigorwritten English proficiency
Certifications
Bachelor's degree