LAVORO SENIOR MANAGER OF STUDY PARMA, EMILIA ROMAGNA

We believe that the success of chiesi is built and shaped by our people and our strong set of shared values and behaviors...   o    cross functional submission team...

Excellent knowledge of the clinical trials settings...  document development: coordinate the writing of informed consent and patient materials, protocol outlines/synopses...

Clinical section of the investigator’s brochure, protocols and clinical study reports)... they will drive the preparation of documents for regulatory submissions...

We promote an environment open to the exchange of ideas and personal and professional growth... join us! your data will be processed in full compliance with the...

We believe that the success of chiesi is built and shaped by our people and our strong set of shared values and behaviors...       assists clinical pharmacology...