Lavoro clinical trial Emilia-Romagna

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...

Select how often (in days) to receive an alert: Clinical Trial Documentation & Records Management Lead Department: Global Clinical Development Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT About us Based in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with...

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 a eTMF Specialist who can join an exciting working environment in a dynamic atmosphere. This position will oversee the global eTMF (electronic Trial...

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...

A leading clinical research organization is looking for a Clinical Trial Manager in Turbigo, Italy. The ideal candidate will manage clinical trial operations, maintain in-depth knowledge of protocols, and provide oversight to project teams. Candidates with expertise in Immunology and Infectious Diseases are encouraged to apply. The position offers remote flexibility, competitive compensation, and...

A leading healthcare intelligence organization is seeking a Clinical Site Associate to support clinical trial operations. The role requires managing site communications, coordinating trainings, and maintaining essential documentation. Ideal candidates will have a Bachelor's in life sciences, experience in clinical research, and strong organizational skills. This position is office-based with...

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...

Evidilya, the dedicated Contract Research Organization of Sprim Health Group operates as a full-service international expertise in successfully developing and managing observational, pre-clinical and clinical trials, is looking for a: Clinical Trial Assistant (STAGE) to reinforce our Operational Team in Milan. Main Tasks: Collaborate and support the study team members for project execution (from...

Medpace is currently seeking candidates withPhDs and/or Post-Doctoral Research experiencefor a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must...

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 a eTMF Specialist who can join an exciting working environment in a dynamic atmosphere. This position will oversee the global eTMF (electronic Trial...

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...

Un'agenzia di staffing globale sta cercando un Clinical Trial Associate a Milano. In questo ruolo, contribuisci al successo delle attività di sviluppo clinico offrendo supporto operativo e amministrativo. Le tue responsabilità includono la gestione delle procedure, l'assegnazione di attività di formazione e il supporto logistico per riunioni. Sono richieste ottime capacità organizzative, fluente...

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...

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 in Immunology and Infectious Diseases are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. We provide remote flexibility...

A global pharmaceutical company is seeking an eTMF Specialist to manage electronic Trial Master File operations. The role requires overseeing eTMF management, ensuring compliance and quality, and leading audit activities. Candidates should have over 5 years of experience in the pharmaceutical or CRO industry and a relevant degree in life sciences. Strong leadership, excellent communication...

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 a eTMF Specialist who can join an exciting working environment in a dynamic atmosphere. This position will oversee the global eTMF (electronic Trial...

A clinical research organization is seeking a Psychiatry Medical Director to lead medical, scientific, and strategic efforts in clinical trials. The role involves providing expertise in study design and safety management while ensuring compliance with research protocols. Ideal candidates should hold an M.D. degree, with preferred experience in clinical trial research and pharmaceutical...

Select how often (in days) to receive an alert: Clinical Trial Documentation & Records Management Lead Department: Global Clinical Development Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT About us Based in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with...

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...

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...