Katalyst Healthcares & Life Sciences
Technical Writer
Katalyst Healthcares & Life Sciences, East Hanover, New Jersey, us, 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:
Make sure to read the full description below, and please apply immediately if you are confident you meet all the requirements.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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Responsibilities:
Make sure to read the full description below, and please apply immediately if you are confident you meet all the requirements.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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