Senior Clinical Trial Associate

Role: Senior Clinical Trial Associate (Sr. CTA) supporting clinical operations for oncology-focused trials. Primary objectives include managing study documentation, vendor coordination, site start-up, and ensuring trial compliance, quality, and timelines. Responsibilities encompass facilitating cross-functional meetings, maintaining regulatory and study documents, developing project timelines, supporting sample management, and collaborating on regulatory submissions. Requirements: Bachelor’s or Master’s degree with at least 3 years of clinical operations experience in pharma or CRO; solid understanding of ICH, GCP, and regulatory standards; strong organizational and attention to detail skills. Preferred skills include experience with clinical trial systems, vendor platforms, and data management. High-value specifics: Oncology therapeutic area, study management, regulatory compliance, GCP, trial documentation, vendor oversight, and cross-functional collaboration. Work setup details are not specified; travel requirements are not indicated.