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Job details

REMOTE | Regulatory Publishing/QC opportunity with a well-funded Rare Disease biotech

This Jobot Job is hosted by Jeff Barron

Are you a fit? Easy Apply now by clicking the "Apply" button and sending us your resume.

Salary $40 - $80 per hour

A Bit About Us

Our client is a publicly traded clinical-stage biotech with a focus on rare disease and orphan drugs in endocrinology. The company's robust pipeline and successful Ph II/III trials have led to strong stock performance and a robust financial runway for continued compound development & pathway to commercialization.

Why join us?

• Make a big impact on small patient populations through the development and approval of orphan drug candidates
• 100% Remote role
• 20 hours per week
• Incredible company culture and proven management team

Job Details

• MS WORD knowledge with WORD styles to format various documents for regulatory submissions
• Adobe Acrobat review and prepare documents for regulatory submission, including bookmarking and hyperlinking
• ECTD publishing experience with using eCTD software to produce a compliant electronic submission

Here's what you'll need

• Bachelor's Degree preferred
• QC experience is a plus
• Work independently to meet submission timelines
• 3+ years of Regulatory Proofreading/Publishing experience within biopharma, medical device, IVD, or CRO industries (protocols, amendments, IBs, CSRs, INDs, NDA modules)
• Strong user of MS Office (Word, Excel, PowerPoint), Adobe Acrobat, and eCTD software

Interested in hearing more? Easy Apply now by clicking the "Apply" button.

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Click our Jobot logo and follow our LinkedIn page!