About the role
At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.
Job Summary
Lead the Global Clinical Operations Team by providing strategic and tactical guidance and support for clinical staff with high degree of quality in the execution of all Global Medical Affairs medical activities in adherence to Good Clinical Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food and Drug Administration (FDA) regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines. Deliver Evidence Generation projects in preparation for launch activities in Oncology Business unit countries as well in other Regions. Responsible for all primary data generation in GMA studies (i.e. Company Initiated Interventional Studies (CIS), Non-interventional Studies (NIS), Expanded Access Programs (EAP), Investigator Initiated studies (IIS) and External Collaborative Study Research projects (ECSR)). Ensure successful execution, timelines and clinical milestones. Accountable for overall Clinical Operation performance against key metrics Accountable for all budget related management