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.
Requirements
- Minimum of a BS degree in life sciences
- Minimum of 4 years of experience editing, formatting, drafting, or reviewing regulatory submission documents
- Excellent interpersonal and communication (verbal and written) skills
- Proficient 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 skills
- Strong understanding of the eCTD and the drug development process
- Proven 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 transparency
- Computer proficiency (Microsoft Office Suite [Word, Excel], Adobe Acrobat, EndNote, and related software) and proficiency in the English language is required
Benefits
- health and wellness programs
- fitness centers
- equity awards
- annual bonuses
- paid time off for eligible employees at all levels
Originally posted on Himalayas
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