Senior Clinical Trial Manager

Role: Senior Clinical Trial Manager responsible for overseeing the operational aspects of multinational clinical trials in biopharmaceutical development. Primary objectives include ensuring trial delivery on time, within budget, and with high quality, while managing site feasibility, vendor coordination, and trial logistics. Responsibilities encompass developing trial documents, site selection, overseeing monitoring and data review, managing timelines and budgets, supply planning, and ensuring compliance with GCP and regulatory standards. The role also involves leading multidisciplinary teams, acting as the main liaison with internal stakeholders, and contributing to process improvements. Qualifications required include a BS/BA in a science-related field, relevant clinical research experience in the biotech/pharma industry, and knowledge of ICH GCP and regulatory requirements. The candidate must demonstrate leadership, project management, and cross-functional collaboration skills, with the ability to manage complex trials across multiple therapeutic areas. Experience in overseeing trials from initiation to reporting and working in a multidisciplinary environment is essential. High-value specifics: involvement in global, large-scale clinical trials in biopharma, with emphasis on GCP compliance, vendor oversight, and cross-team coordination. Location: not specified; work environment and travel requirements are not detailed.