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Work from Office
Full Time
Coordinate and oversee the operational aspects of global clinical trials, ensuring compliance with regulatory requirements, study protocols, and company standards.
Support trial start-up activities, including site selection, contract negotiations, and ethics submissions across multiple geographies.
Monitor trial progress by maintaining close communication with investigators, vendors, and cross-functional teams to ensure timelines, quality, and budget targets are met.
Manage and track essential trial documentation in accordance with Good Clinical Practice (GCP) and internal procedures.
Facilitate resolution of operational issues by collaborating with internal stakeholders and external partners.
Assist in the development and review of trial-related materials such as investigator meeting presentations, training guides, and monitoring plans.
Ensure accurate and timely reporting of trial metrics, risks, and progress to project leadership.
Contribute to process improvement initiatives to enhance the efficiency and quality of global trial execution.
Bristol Myers Squibb
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