LAVORO DIRECTOR OF CLINICAL RESEARCH PARMA, EMILIA ROMAGNA

clinical section of the investigator’s brochure, protocols and clinical study reports)...       strong understanding of gcp, regulatory requirements, and clinical...

Strong knowledge of ich-gcp, clinical trial lifecycle, regulatory requirements, and cro/vendor management... languages fluency in english technical skills excellent...

Strong understanding of gcp, regulatory requirements, and clinical trial methodologies... experience required significant experience in designing and executing...

Purpose the redeo (r&d external opportunity) leader will spearhead the evaluation of preclinical, clinical or commercial stage external opportunities from the evaluation...

Purpose of the role: improving the lives of patients through innovative clinical research...    passion for improving the lives of patients through innovative...

Support the definition and periodic refresh of the r&d strategy through the collection and elaboration of both qualitative and quantitative information...

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

Basic knowledge of python (e... participating in the analysis and interpretation of computational results, under the guidance of senior scientists...

Deep knowledge of gmp/cgmp and guidelines (ich, emea, pqri, health canada) related to the pharmaceutical development of inhalation products...

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...

Maintain detailed and accurate records of experiments and results... design, develop, and execute in vitro pharmacological assays to evaluate the efficacy and mechanism...

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...