Global Clinical Trial Manager | Country Lead

A leading biopharmaceutical company is seeking a Clinical Trial Manager in Rome. The role involves overseeing clinical studies in Italy and coordinating with stakeholders. Candidates should have a Bachelor's or Master's degree in life sciences and at least four years of relevant experience in clinical research. Excellent organizational and communication...

Clinical Trial Manager – RomeJoin to apply for the Clinical Trial Manager role at Bristol Myers Squibb .About the RoleThe Clinical Trial Manager (CTM) is accountable for end‑to‑end study operational oversight and delivery at country level (Italy, Greece, Israel and Croatia), ensuring adherence to timelines, budget and quality standards. Acts as the...

Clinical Trial Documentation & Records Management Lead Join to apply for the Clinical Trial Documentation & Records Management Lead role at Chiesi Group 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)....

Clinical Trial Documentation & Records Management Lead Join to apply for the Clinical Trial Documentation & Records Management Lead role at Chiesi Group 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...

Clinical Trial Documentation & Records Management LeadJoin to apply for the Clinical Trial Documentation & Records Management Lead role at Chiesi GroupBased 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...

A global pharmaceutical company based in Parma, Italy is seeking a Clinical Trial Documentation & Records Management Lead. This role requires leadership in managing clinical documentation and records, ensuring compliance with regulatory standards, and overseeing clinical trial technologies. Candidates should have 8-10 years of experience in clinical...

A global pharmaceutical company based in Parma, Italy is seeking a Clinical Trial Documentation & Records Management Lead. This role requires leadership in managing clinical documentation and records, ensuring compliance with regulatory standards, and overseeing clinical trial technologies. Candidates should have 8-10 years of experience in clinical...

We aspire to be the premier research-intensive biopharmaceutical company in the world. We demonstrate our commitment to patients and population health by increasing access to health care through far-reaching policies, programs, and partnerships. Today, we continue to be at the forefront of research to prevent and treat diseases that threaten people and...

Working with Us Challenging. Meaningful. Life‑changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

Working with Us Challenging. Meaningful. Life‑changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...