Scientific Writer

We are hiring Scientific Writer.Please let me know if you are interested or anyone who might be interested.Client: Major Agriscience ClientPosition: Scientific WriterDuration: 12 Months ContractLocation: Newark DE 19711Pay Rate: $30.00-$34.00/ Hr on W2____________________________________________________________________________________________Description:This is a Scientific Writer contractor position supporting Global Regulatory Science Operations. The Scientific Writer will be responsible for drafting and finalizing toxicology protocols, study reports, and study summaries to support regulatory submissions.The role requires strong scientific writing skills, a solid understanding of Good Laboratory Practice (GLP), and the ability to collaborate effectively with cross-functional stakeholders.Preferred Skills & Experience:Bachelor’s degree in Biology, Microbiology, or a related scientific discipline Prior experience with scientific writing and GLP preferred Ability to manage multiple projects simultaneously and meet tight deadlines Strong attention to detail Experience using Adobe Acrobat Pro to compile and edit documents preferred Proficient in Microsoft Office Suite and document management systems Job SummaryDraft high-quality toxicology protocols, study reports, and study summaries to support regulatory submissions Utilize strong scientific writing skills with a background in toxicology or related biological sciences Perform quality control (QC) reviews on draft reports with an understanding of Good Laboratory Practice (GLP) Contribute to the development and revision of report templates and assist with process optimization efforts Facilitate finalization of reports and audit responses Communicate effectively with key stakeholders Partner with stakeholders to understand regulatory reporting requirements Job RequirementsBachelor’s degree or higher in Biology, Microbiology, or a related scientific discipline Demonstrated experience in scientific writing, preferably within a regulatory environment Strong understanding of Good Laboratory Practice (GLP) standards and regulatory guidelines Excellent attention to detail with the ability to perform quality control reviews Proficiency in Microsoft Office Suite and document management systems Strong communication and collaboration skills Ability to manage multiple projects and meet tight deadlines Experience using Adobe Acrobat Pro is preferredRegardsVishnu Das Natesandvishnu@radiants.com