The candidate assuming this position will be responsible for executing activities related to the clinical development of a medical device used for the treatment of malignancies. The job will involve an analytical review of data, as well as the development of reports, protocols and other tools, to be used internally and externally. In order to successfully accomplish relevant assignments, collaboration with other teams within the company and with external medical teams will be required.
Critical evaluation of literature, standard practices and internal data to support the development of new clinical studies
Analysis of technical and clinical data generated using clinical trials for the purpose of creating publications, guidelines and tools.
Medical support for regulatory submissions globally as needed.
Support to other teams on clinical development topics, as required.
Experience in clinical trial management, clinical development or in the biomedical industry is an advantage but not a requirement
Excellent verbal and written communication skills in English (mother tongue-level) are a must.
Ability to work both independently and in collaboration with peers.
Proficiency in Microsoft Office (Word, Excel, PowerPoint).