Senior Clinical Trial Manager

Role: Senior Clinical Trial Manager overseeing a global Phase 3 oncology trial, responsible for project leadership from initiation to closeout, vendor management, and regulatory compliance. Key responsibilities include managing vendors (CROs, labs, eTMF), ensuring trial progress within scope, budget, and quality standards (GCP, SOPs), overseeing data integrity, and facilitating cross-functional communication. The role involves contract negotiations, site feasibility, protocol review, and audit readiness. Qualifications: 5-7 years of clinical trial experience with proven management of Phase 3 studies, preferably in oncology, with a BA/BS in a relevant field. Requires strong knowledge of ICH, GCP, and regulatory requirements, excellent communication skills, and ability to multitask. Travel may be required. High-Value: global Phase 3 oncology, vendor oversight, regulatory compliance, cross-functional coordination, trial lifecycle management.