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Associate Medical Writer

DBV Technologies • NJ, US • published 2026-11-05 06:59:20.725359

Description

**Description :** ----------------- DBV Technologies is seeking a detail\-oriented Associate Medical Writer/QC Specialist to support the development of clinical trial documents and regulatory submissions. The ideal candidate will demonstrate writing experience and full quality control capabilities in developing clinical study reports, protocols, Investigator’s Brochures, DSURs, and related documents. This role focuses on scientific writing and meticulous document compilation. The successful candidate will optimize SharePoint document organization, work efficiently under shortened deadlines, and communicate proactively with stakeholders to ensure adherence to established timelines. Additional responsibilities may be assigned depending on project needs and organizational priorities. **Location** : Warren, New Jersey \- minimum 3 days on site **Salary Range** : $85\-110k **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 (QC) reviews of deliverables, including e...

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