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
Sei pronto per entrare a far parte di una società di consulenza leader mondiale nellindustria farmaceutica e dei Medical Device? PQE Group opera con successo in questo settore dal 1998, garantendo una presenza internazionale grazie a
About usChiesi 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
On behalf of our Client, a biopharmaceutical company, IQVIA, a global leader in services for the pharmaceutical and biotechnology industries, is seeking for a Marketing Support Specialist based in Milan. Work area: Milan; The Marketing Support
On behalf of our Client, Chiesi Farmaceutici , one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for a
Global Regulatory Affairs Manager-Maternity Cover IQVIA Italia•Emilia-Romagna, Italy On behalf of our Client, Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and
IQVIA Italia in Milan is seeking a Marketing Support Specialist to contribute to the success of AHP and PH1 Programs within the International Rare Brand Team supporting operational activities. The role involves coordinating cross‑functional projects, localizing
Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last
Overview In this role you will drive the digital transformation of R&D by aligning processes, data and technology. You act as a strategic connector across functions to design and implement end-to-end, data-driven processes enabled by platforms
Overview In this role you will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. You will work within a regulatory team to shape submission strategies, assess quality-related changes, and coordinate cross-functional