Senior Editor
The Senior Editor will independently review or supervise quality control of nonclinical regulatory submission documents, maintain lists of QC comments, and collaborate with writing staff across therapeutic areas.RequirementsMinimum of a BS degree in life sciencesMinimum of 4 years of experience editing, formatting, drafting, or reviewing regulatory submission documentsExcellent interpersonal and communication (verbal and written) skillsProficient in use of all software required for document drafting as well as document management platforms (eg, SharePoint and Veeva Vault RIM)Sophisticated verbal and graphical data presentation skillsStrong understanding of the eCTD and the drug development processProven understanding of bioanalytical sciences and nonclinical subject matter supporting drug development (ie, pharmacokinetics, pharmacology, and toxicology) and ability to communicate this information with precision and transparencyComputer proficiency (Microsoft Office Suite [Word, Excel], Adobe Acrobat, EndNote, and related software) and proficiency in the English language is requiredBenefitshealth and wellness programsfitness centersequity awardsannual bonusespaid time off for eligible employees at all levelsOriginally posted on Himalayas
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