What are the responsibilities and job description for the Technical Writer position at Katalyst Healthcares & Life Sciences?
Company Description
- 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
- 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
- regulatory bodies.
- Ability to work within cross-functional teams.
Additional Information
All your information will be kept confidential according to EEO guidelines.
