Line of ServiceAdvisory Industry/SectorNot Applicable SpecialismCybersecurity & Privacy Management LevelIntern/Trainee Job Description & SummaryAt PwC, our people in cybersecurity focus on protecting organisations from cyber threats through advanced technologies and strategies. They work to identify vulnerabilities,
If you are an experienced Senior CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you! Translational Research in Oncology (TRIO) is 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, 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
In this role you lead strategic delivery of global clinical trials, partnering with sponsors and cross-functional teams to accelerate development of innovative therapies. You guide multi-regional studies, ensuring quality, timelines and budget alignment while navigating regulatory requirements. You
TGR Haas F1 Team has been a stalwart of the FIA Formula 1 World Championship over the past decade. With more than 200 grand prix starts to our name, we pride ourselves on being an ambitious
Select how often (in days) to receive an alert: Department: Global Regulatory Affairs & Patient Safety Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT About us Chiesi is an
TGR Haas F1 Team has been a stalwart of the FIA Formula 1 World Championship over the past decade. With more than 200 grand prix starts to our name, we pride ourselves on being an ambitious
About Us Based in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with 90 years’ experience, operating in 31 countries with more than 7,000 employees (Chiesi Group). To achieve its mission of improving
Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in our Milan office. Clinical Trial Managers with expertise
Upstream Biological Process, Lead Scientist Date: 2 Jul 2026 Business Area: Industrial Operations & HSE Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT About us Chiesi is an international research-focused biopharmaceutical group with 90
Clinical Contracts Associate – Italy Location: Remote, Italy – open to candidates based anywhere in Italy Employment Type: Full-Time, 12-Month Fixed-Term Contract Hours: 40 hours per week Start Date: To be confirmed Project Status: Pipeline opportunity,
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Department: Global Clinical Development Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Europe, IT Purpose An accomplished clinical development
Project Development Manager – Solar PV & BESS (Hybrid) This is an opportunity to join a well-funded and fast-growing renewable energy developer with operations across multiple European countries. The company is delivering high-quality solar PV and
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
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
IQVIA seeks an Experienced Clinical Research Associate to work from home in Italy. You will perform site monitoring and site management to ensure studies are conducted per protocol, GCP, and ICH guidelines. You will coordinate monitoring visits
IQVIA is seeking an Experienced Clinical Research Associate, Site to perform monitoring and site management duties needed to ensure studies are conducted according to protocol, GCP, ICH guidelines, and sponsor requirements. You will conduct site visits—from selection
As an energy park developer, the UKA Group plans, builds, operates, and sells wind, photovoltaic (PV) and battery storage projects. It contributes to a sustainable power supply in Germany, Europe and America that is independent of
Chiesi Farmaceutici S.p.A. is seeking a Real World Evidence Lead Endo-Metabolic to drive the global RWE strategy for the Endo‑Met portfolio within GRD. You will shape the integrated evidence plan, align with cross‑functional teams, and advance