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
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
At Genmab, we are dedicated to building extraordinary futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create,
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
Responsible for the implementation and the optimization of robust manufacturing processes in Production ensuring that safety, effectiveness, quality and reliability of the devices are met. Lead PFMEA activities in coordination with other stakeholders. Generate and validate
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 Clinical
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 Clinical
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
Department: GRD Regulatory Affairs Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT Principal Regulatory Writer, Global Rare Diseases Chiesi is an international research-focused biopharmaceutical group with 90 years’
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 Clinical
Are you a talented Clinical Trial Assistant with a passion for clinical research? Were looking for an experienced Freelance CTA to join a dynamic team supporting cutting-edge studies Key Responsibilities: Assist in the management and oversight of
Financial Assistant - Graduate Hiring 2025 / 2026 Direct message the job poster from Midea Group Job Type: Fixed Term Contract, Full Time Reports To: NetherlandsTeam Leader, Financial Shared Service EMEA Languages Required: English, Mandarin and Italian
Experteer OverviewIn this role you drive the operational management of assigned clinical projects, ensuring alignment with Chiesi’s goals and medical standards. You will coordinate with CROs, internal partners, and vendors to deliver studies on time and
Select how often (in days) to receive an alert: Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Italy, IT About us Chiesi is an international research-focused biopharmaceutical group with 90