With over 120 years of experience and approximately 19,000 employees in more than 30 countries/regions, Daiichi Sankyo is dedicated to discovering, developing, and delivering new standards of care that enrich the quality of life around the world.
In Europe, we focus on two areas: The goal of our Specialty Business is to protect people from cardiovascular disease, the leading cause of death in Europe, and help patients who suffer from it to enjoy every precious moment of life.
In Oncology, we are driving innovation in solid tumours and blood cancers, founded on breakthrough science from our own labs in Japan. We aspire to create better tomorrows for people living with cancer and their loved ones.
Our European headquarters are in Munich, Germany, and we have affiliates in 15 European countries and Canada.
We are seeking highly qualified candidates to fill the position:
Director Global Oncology Medical Affairs (m/f/x) - Clinical Trial Management
The position:
Lead and drive execution and project management of Global Oncology Medical Affairs (GOMA) clinical activities, in adherence to Good Clinical Practice (GCP), appropriate Standard Operating Procedures (SOPs), Food and Drug Administration (FDA) regulations/EU Clinical Trials Regulation, and International Conference on Harmonization (ICH) guidelines. The types of clinical activities include company sponsored studies (interventional and non-interventional) as well as medical affairs research projects.
The job holder will take responsibility for the clinical operational strategy and overall delivery (i.e. Project Lead role) of clinical studies (incl. vendor management and oversight) and will represent GOMA Clinical Operations on the GOMA program and study team. This position requires project management in a global and multi-functional matrix environment and may require future line management responsibility of Clinical Trial Managers. The Director will be expected to take both strategic and tactical roles to effectively deliver clinical studies and projects in time, with full compliance, and with highest quality. At this level, the incumbent may be expected to lead a program of studies.
Representative and interface for all study related Clinical Operation tasks and activities of the GOMA program team(s) and with alliance partner(s).
The job holder will also work on GOMA clinical operations processes and systems related developments, implementations, and maintenance as well as on applicable training and SOP settings.
The Director will be expected to work in a collaborative, global environment, and demonstrates excellent collaborative interactions and proactive communication with all relevant global partners and functions as well as across regional locations.
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