Clinical Operations Manager
CurrentTherapeutic Area: Lung, Breast and Brain cancer.• Leading local and global coordination of clinical trial (phase II-III) activities covering startup, maintenance and closeout.• Setting up and managing external providers (third-party vendors) involved in activities such as supplies, central Lab, translation, and meeting planners. • Contributing significantly to the development of protocol and study guidelines; as well as internal documents such as SOPs, WINs..• Accountable for overseeing study planning, defining timelines, and ensuring the timely attainment of estimated milestones.• Responsible for site management aspects (selection, training, recruitment, support for samplescollection and drug management, closure).• Regularly reporting on the study status during project-based meetings and contributing to the creation and maintenance of Project Logs and Risk Management Plans (RMPs).• Working closely within a cross-functional international study management team, particularly with Project Managers, Regulatory Affairs Managers, and Clinical Research Physicians/Clinical Scientists.• Leading, supporting, and motivating study teams to elevate their performance to ensure high-quality and timely project deliverables.• Organizing and conducting investigator meetings and group meetings with key opinion leaders (KOL). Being part of the board committee of the EORTC Lung Cancer Group. • Collaborating with internal and external stakeholders for study-related activities or global operational activities.
