A leading pharmaceutical company is seeking a Clinical Trial Manager to oversee study operations in Italy, Greece, Israel, and Croatia. The ideal candidate will have a bachelor's or master's degree in life sciences and at least 4 years of relevant experience. Responsibilities include coordinating with global teams, managing patient recruitment strategies, and ensuring compliance with clinical...
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 the lives of patients, and the careers of...
A leading pharmaceutical company is seeking a Clinical Trial Associate (CTA) in Turbigo, Italy, to provide operational support to the global clinical team. The role is vital in maintaining quality systems and documentation compliance. Ideal candidates will have a Bachelor's degree in a related field and be fluent in both English and Italian. Experience in clinical research and familiarity with...
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 operations and leadership skills, as well as...
Sr. Clinical Trial Manager (Clinical Research Medical Advisor) - FSP - Homebased - ItalyUpdated: January 5, 2026Location: ITA-RemoteJob ID:25104909DescriptionSr. Clinical Trial Manager (Clinical Research Medical Advisor) - FSP - Homebased - ItalySyneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical,...
A leading pharmaceutical company is seeking a Clinical Trial Documentation & Records Management Lead in Parma, Italy. This role involves establishing and improving the documentation unit, ensuring compliance with regulatory standards. Ideal candidates will have 8-10 years of clinical operations experience, strong leadership skills, and knowledge of eTMF and CTMS systems. Flexible hybrid working...
A leading life sciences company in Italy seeks a Clinical Study Administrator to coordinate study activities and manage trial documentation in compliance with regulatory standards. The ideal candidate will have a Bachelor’s degree in a related field, along with at least 2 years of relevant experience. Strong collaboration, organizational skills, and proficiency in MS Office are essential. The...
A leading healthcare company is seeking a Manager for Trial Delivery Management in Turbigo, Italy. This role involves overseeing the execution of clinical trial activities, vendor management, and mentoring team members. Candidates should possess a BS in Life Sciences and have at least 8 years of relevant experience in the pharmaceutical or healthcare sectors. Strong leadership and project...
A leading clinical research organization in Turbigo, Italy, seeks a Clinical Research Physician responsible for providing medical leadership for clinical trials. The role involves developing new projects, managing safety issues, and coordinating with various departments. Candidates must have an M.D. degree and prior clinical trial experience. The position offers hybrid work flexibility and...
A global healthcare company is seeking a Clinical Trial Coordinator in Verona, Italy. The role involves assisting the clinical research team in conducting studies aligned with GCP and other protocols. Key responsibilities include managing start-up activities and document management, maintaining relationships with ethical committees, and ensuring compliance with regulatory requirements. Ideal...
A renowned Contract Research Organization in Milan is seeking a Clinical Trial Assistant to support project execution from start to finish. The ideal candidate will have a Master’s Degree in a scientific discipline or health care, possess strong organizational and decision-making skills, and be fluent in English. This role involves managing study documents, evaluating study sites, and...
Select how often (in days) to receive an alert:Clinical Trial Documentation & Records Management LeadDepartment: Global Clinical DevelopmentBusiness Area: R&D, Pharmacovigilance & Regulatory AffairsJob Type: Direct EmployeeContract Type: PermanentLocation: Parma, ITAbout usBased in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare 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 within the pharmaceutical and biotechnology industry a global pharmaceutical company - IQVIA is looking for aeTMF Specialistwho can join an exciting working environment in a dynamic atmosphere.This position will oversee the global eTMF (electronic Trial...
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 achieve its mission of improving people’s...
Job OverviewMedpace 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 Italy, particularly in our Milan office. Clinical Trial Managers with expertise in Neuroscience and CNS are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. We...
Sr. Clinical Trial Manager (Clinical Research Medical Advisor) - FSP - Homebased - ItalyUpdated: January 5, 2026Location: ITA-RemoteJob ID:25104909DescriptionSr. Clinical Trial Manager (Clinical Research Medical Advisor) - FSP - Homebased - ItalySyneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical,...
A leading pharmaceutical company in Parma, Italy, seeks a Clinical Trial Documentation & Records Management Lead to ensure compliance with regulatory standards and manage clinical trial technologies. The ideal candidate has 8-10 years of experience in clinical operations and a robust understanding of eTMF and CTMS. This role emphasizes team leadership, cross-functional collaboration, and...
Planet Pharma is seeking a Clinical Trial Associate (CTA) to provide key operational and administrative support to a global Clinical team. This role plays an important part in maintaining quality systems, training compliance, documentation and clinical platforms, helping to ensure efficient and compliant clinical development activities.Key ResponsibilitiesMaintain and regularly update SOP...
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 skills are necessary to ensure compliance...
A leading pharmaceutical company is seeking a Clinical Trial Associate (CTA) in Turbigo, Italy. In this vital role, you will support the global clinical team, ensuring quality systems and documentation compliance. Ideal candidates should have a Bachelor's degree in a related field and be fluent in English and Italian. Experience in clinical research and familiarity with SAP Success Factors is...