Exciting oncology drug development company with a solid pipeline is currently looking to expand their clinical development team in Italy with a new pivotal Oncology Clinical R&D role.
You will develop clinical protocols, manage clinical studies, and work cross-functionally with Clinical Operations, Data Management, Statistics, Regulatory, Pharmacovigilance, and Quality Assurance to ensure study start-up activities, study oversight, and reporting of the assigned oncology clinical trials. You will represent the Clinical Sciences team in internal governance and committee meetings relating to the overall clinical development strategy and operational study implementation, and at external meetings including FDA/EMA interactions and other national regulatory agencies.
With a medical degree and oncology clinical research or clinical practice, you have industry or (sub)investigator experience in a clinical development setting. If being part of a united team and new therapeutic approaches to oncology and malignant haematology drug development are key professional drivers for your career, please send your application.