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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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