Quality Control Specialist

Key responsibilities: Perform quality checks, copyediting, and proofreading of clinical and regulatory documents to ensure accuracy and compliance Manage multiple projects simultaneously, adhering to tight timelines and communicating effectively with Medical Writers Build partnerships with intradepartmental teams and engage in training to enhance knowledge of medical writing and regulatory requirementsRequired qualificationsBA/BS degree; advanced degrees such as a Masters, PhD/PharmD are a plus At least 1 year of relevant experience in QC editing, medical writing, or technical copyediting Experience with pharmaceutical industry regulatory documents, including clinical study reports and protocols Familiarity with drug/biologics development processes and regulatory submission requirements Technical expertise in Microsoft Office Suite and Adobe Acrobat; familiarity with SharePoint and Veeva Vault is a plus