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Medical Writer

DBV Technologies • NJ, US • published 2026-11-05 06:59:20.725398

Description

**Description :** ----------------- DBV Technologies is seeking a skilled and detail\-oriented Medical Writer to support the development of clinical trial documents and regulatory submissions. This role focuses on scientific writing in accordance with regulatory guidelines. The ideal candidate has extensive writing experience developing clinical study reports, protocols, Investigator’s Brochures, DSURs, regulatory submissions (BLA/NDAs), and related documents. The successful candidate will work efficiently under shortened deadlines, communicate proactively with stakeholders to ensure adherence to established timelines, and be able to read and summarize efficacy and safety data in succinct, regulatory\-compliant language. Additional responsibilities may be assigned depending on project needs and organizational priorities. **Location** : Warren, New Jersey \- minimum 3 days on site **Salary Range** : $105\-130k **Key Responsibilities :** -------------------------- * Support the development of clinical documents that are compliant with regulatory guidelines, including preparation of redlined versions and summary of changes documents as required. * Perform comprehensive quality control...

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