10 set - Ancona
Biopharma Careers
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 singular purpose: promoting a healthier world for our people, patients, and the planet. This is what drives us as we research, develop, and market innovative drugs across our main therapeutic areas. Discover more here.
Chiesi Global Rare Diseases Chiesi Global Rare Diseases is a Chiesi Group’s business unit established in February 2020 and focused on research, development and commercialization of treatments and patient support services for rare and ultra-rare disorders, many of whom have limited or no treatments available.
This unit is based in Boston, Massachusetts, with a strong synergy with the headquarters in Parma.
Rare unit has a focus on research and product development for lysosomal storage diseases, rare hematology, ophthalmology disorders and rare immunodeficiencies.
The unit is also a dedicated partner with global leaders in scientific research, patient advocacy and care. Discover more here.
What we are looking for This is what you will do
- Support the clinical team in relevant medical and scientific aspects of the assigned global clinical studies within the global clinical development program
- Contributes to the risk/agevolazioni assessment of the ongoing clinical trials assigned
- May act as the primary medical monitor for an assigned clinical study
- Contributes to the production of the Common Technical Document, in terms of validation of scientific documents relevant to the assigned clinical study (e.g. study protocol, investigator’s brochure, clinical study reports) and represents the company in front of health authorities, partners and institutions
- Develops and enhances the management of the clinical trials, working in collaboration with the Clinical Program Leader and other relevant roles and ensures medical and sci
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