Newark Metro Area, New Jersey
1. Collaborate with translational scientists and appropriate representatives from various scientific
disciplines (Pharmacology, Toxicology, Drug Metabolism & Pharmacokinetics) for compiling and writing pre-clinical and translational manuscripts and other scientific documents such as study reports, pre-clinical and translational sections for regulatory submission dossier
2. Review data to determine the appropriate tabular and textual formats, and the clarity, logic and
order of presentation.
3. As needed, review work of other writers for accuracy, quality, focus, and
adherence to format and stylistic requirements in order to ensure high quality documents
4. Other duties as assigned
Advanced degree in biological or related sciences (MS or PhD).
Excellent scientific writing and verbal communication skills. Demonstrated ability to compile
concise summaries of complicated data sets.
Expertise and knowledge in pre-clinical/translational writing
More than 5 years of previous experience in independently authoring scientific publications,
reports, and/or review articles, preferably in pharmaceutical related fields.
Advanced skills in use of Microsoft Word, Excel, data graphics software, Adobe Acrobat, and
web-based browser software such as LiveLink to manage electronic document authoring,
reviewing, and approval process.
Knowledgeable in pre-clinical development and translational sciences
Advance knowledge of document guidelines for regulatory submission to FDA and other global
Ability to work within cross-functional teams.