Senior Medical Writer

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Posted 11 days ago United States Salary undisclosed
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Job Description

Role Senior Medical Writer Location Summit, NJ(Remote Start) Duration 12+ months BASIC RESPONSIBILITIES We seek an individual with a strong scientific background and experience in writing manuscripts for publication in peer-reviewed journals. The successful candidate will join a cross-functional publication team to develop, manage and execute publication plans of one or more therapeutic areas in support of clinical programs in HematologyOncology. Responsibilities include timely and efficient planning, development, and submission of manuscripts, abstracts, and scientific meeting presentations, in partnership with company teams (scientists, study investigators, other writers and medical communications) and publication vendor. Additional responsibilities include assisting in preparation of other scientific documents, including clinical and non-clinical study reports, as well as preclinical and translational sections for regulatory submission dossier. The position requires a self-motivated, independent worker, able to balance several projects and assignments and deliver materials on deadline. The successful candidate will possess an understanding of pre-clinical development and translational sciences, including biomarkers, and working knowledge of basic medical statistics. Excellent communication skills with an ability to effectively convey scientific concepts concisely and accurately are absolutely required. SPECIFIC DUTIES bull Collaborate with translational scientists and representatives from various scientific disciplines (HematologyOncology, Pharmacology, Drug Metabolism Pharmacokinetics) to develop, manage and execute publication plans with a focus on preclinical development and translational sciences. bull Contribute to the development, review, approval, and submission of manuscripts for publication in peer-reviewed journals and at key independent medical and scientific congresses bull Review data to determine the appropriate tabular and textual formats, and the clarity, logic and order of presentation. bull Assist in the preparation of other scientific documents, including clinical and non-clinical study reports, preclinical and translational sections for regulatory submission dossier. bull 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. SkillsKnowledge Required bull Advanced degree in biology, pharmacology, or related science (MS or PhD). bull At least 3 years of experience in writing scientific publications, abstracts, reports andor review articles in biological or pharmaceutical research related fields. bull Excellent technical scientific writing and verbal communication skills. bull Knowledgeable in preclinical development and translational sciences, including biomarkers. bull Demonstrated ability to compile concise and accurate summaries of complicated data sets. bull Working knowledge of basic medical statistics. bull Proficiency in use of Microsoft Word, Excel, Adobe Acrobat, data graphics software, and Spotfire. bull Advanced knowledge of and compliance with Good publication practices and ICMJE guidelines. bull Demonstrated ability to work on multiple projects efficiently and in a timely manner. bull Ability to work within cross-functional teams. Please email resumes to david(at)aethonsolutionsllc.com mailto Thanks and Regards, David Aethon Solutions, LLC Email david(at)aethonsolutionsllc.com mailto