Quality Control Specialist, Medical Writing

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Quality Control Specialist, Medical Writing based in United States. This role is responsible for ensuring the accuracy, consistency, and quality of clinical and regulatory documents throughout the medical writing process. You will review critical documentation supporting clinical development and regulatory submissions, including study reports, protocols, investigator’s brochures, and submission materials. The position combines scientific review, technical editing, proofreading, data verification, and quality control within strict project timelines. You will collaborate closely with medical writers and cross-functional teams to maintain high documentation standards. The role also provides opportunities to deepen knowledge of medical writing, medical terminology, drug and biologics development, and regulatory requirements. This is a full-time remote opportunity suited to a detail-oriented professional who thrives in a collaborative and fast-paced environment.