About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a
Experteer Overview In this role you will author, review, and manage regulatory documents that translate clinical, nonclinical, and CMC data into compliant submissions for global authorities. You will serve on cross‑functional teams to ensure scientific rigor and
Experteer Overview In this role you drive GCP compliance within clinical development, acting as a QA reference for project teams. You’ll implement and maintain the quality system in GCP areas and support study design, execution, and
Experteer Italy seeks a candidate to author and manage regulatory documents that translate data into compliant submissions. This role involves overseeing document development for marketing applications and guiding both external writers and internal experts. The ideal candidate
Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular purpose: