LAVORO OVERALL STUDY OF THE PARMA, EMILIA ROMAGNA

Supervise to guarantee the compliance of the validation processes and collaborate on the drafting of validation project plans and validation final reports...

Purpose of the role: improving the lives of patients through innovative clinical research... drive the implementation of dei (diversity, equity and inclusion)...

these units are responsible for the development and implementation of the therapeutic area strategies... the intern will report to the gva global pricing sr analyst...

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...

Provide clinical leadership within the core team, ensuring the clinical perspective informs key strategic decisions... we believe that the success of chiesi...

the members of kpmg’s ctr team support organisations across all phases of the process to ensure the security of their information and business strategies...

Clinical section of the investigator’s brochure, protocols and clinical study reports)... they ensure scientific and medical integrity in the development and execution...

We believe that the success of chiesi is built and shaped by our people and our strong set of shared values and behaviors...   who we are looking for purpose the...

Ensure overall gra project timelines are aligned cross-ta / cross-functional teams and support the coordination of timely regulatory submissions...

We believe that the success of chiesi is built and shaped by our people and our strong set of shared values and behaviors... study experience abroad would be consider...

As a result of our commitment to fostering an  inclusive work  environment, our network complies with the standards of the iso requirements, on the diversity and...