Clinical Study Manager in Oncology

Elevate your career in clinical trials with a Global Study Manager role focused on oncology. Utilize your end-to-end execution skills and clinical trial experience to drive impactful studies. Join a dynamic team responsible for managing global clinical trials through their entire lifecycle. Leveraging at least three years of clinical trial experience in the pharma sector, this role emphasizes strong project management skills including budget handling and timeline adherence. Your leadership will coordinate efforts across diverse teams ensuring studies meet their key deliverables. Key Responsibilities:

• Lead global clinical trial lifecycle from start-up to closeout
• Manage timelines, budgets, and study deliverables efficiently
• Partner cross-functionally with DM, Regulatory, Safety, and vendors
• Track enrollment, data delivery, and overall trial progress
• Oversee vendor performance and scope management

Requirements:

• 3+ years of experience in clinical trials, especially in oncology
• Bachelor’s degree in life sciences or a related field
• Hands-on experience with TMF and CTMS systems
• Solid understanding of ICH-GCP and drug development
• Leadership experience with CROs and external vendors

Utilize your expertise in trial management to deliver excellence in oncology research. #J-18808-Ljbffr