Global Study Management Associate (gSMA)

Role: Clinical Study Coordinator supporting global clinical trial delivery in oncology-focused biopharma. Responsibilities: assist the Clinical Study Manager with study planning, logistics, document management, and cross-functional collaboration; support site feasibility, monitor key study metrics, prepare reports, and maintain systems like eTMF and CTMS. Ensure compliance with GxP, ICH-GCP guidelines, and quality standards; support study drug supply planning and data cleaning activities. Qualifications: Bachelor's degree in a scientific or healthcare discipline; 1+ year experience in clinical research within biotech, pharma, or CRO; proficiency in MS Office and clinical systems; knowledge of clinical operations and regulatory guidelines. Preferred: higher degree in a relevant field. High-Value: involvement in oncology clinical trials, supporting study execution from planning through data management in a global setting. Collaboration: work with global Clinical Study Manager, regional trial associates, vendors, and study teams. Work setup: limited travel, primarily office-based. Focus on supporting study quality, timelines, and budgets in a fast-paced oncology environment.