Description
QPS is hiring a Clinical Trial Associate to support the full lifecycle of clinical studies, including project operations, meeting coordination, document management, quality and compliance monitoring, finance support, and site initiation and tracking. The role requires clinical research or related experience, strong organizational and communication skills, Veeva Vault and clinical tracking-system experience, and Microsoft Office proficiency. It is 100% home-office based, may require up to 5% travel, and includes benefits such as a company-matched 401(k), life and disability insurance, and advancement opportunities.
