Katalyst Healthcares & Life Sciences
Technical Writer Job at Katalyst Healthcares & Life Sciences in East Hanover
Katalyst Healthcares & Life Sciences, East Hanover, NJ, United States, 07936
- Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
- We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.
Job Description
Responsibilities:
- 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.
- Review data to determine the appropriate tabular and textual formats, and the clarity, logic and order of presentation.
- 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.
- Other duties as assigned.
Skills/Knowledge Required:
- 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 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 regulatory bodies.
- Ability to work within cross-functional teams.
Additional Information
All your information will be kept confidential according to EEO guidelines.
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