Lavoro Clinical Trial Manager Emilia-Romagna

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...

Sr. Clinical Trial Manager (Clinical Research Medical Advisor) – FSP – Homebased – Italy Join to apply for theSr. Clinical Trial Manager (Clinical Research Medical Advisor) – FSP – Homebased – Italyrole atSyneos Health. Company Overview Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical...

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...

Un importante ospedale di ricerca a Milano cerca un Data Manager per il progetto 'Prehabilitation to improve heart Rate variability In surgical cancer patients'. Il candidato si occuperà della gestione dei dati, redazione di report e inserimento delle informazioni cliniche. È richiesta laurea magistrale in Biologia o titolo equivalente e si offre un contratto di collaborazione con un trattamento...

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 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...

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 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 global biopharmaceutical organization is looking for a Sr. Clinical Trial Manager to ensure the execution of clinical trials in Italy. This role requires providing medical and scientific leadership, auditing regulatory compliance, and collaborating with cross-functional teams. Candidates should have a Medical Doctor degree or a related Pharma degree and at least 3 years of experience in...

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...

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...

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...

Job Overview 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 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...

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...