Clinical Trial Associate
17 ore fa
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 Responsibilities Maintain and regularly update SOP inventories, training matrices and compliance documentation. Coordinate, assign, track and document training activities in line with regulatory and internal requirements. Support clinical administrative processes including CV management, onboarding documentation, vendor tracking and organizational charts. Manage system access and user coordination for platforms such as eTMF, Veeva QDocs and DocuSign, working closely with IT and internal stakeholders. Assist with the planning and coordination of internal and external meetings, ensuring logistics, materials and documentation are prepared. Serve as first-line support for basic system and access-related issues, ensuring clear and effective communication with relevant teams. Qualifications & Skills Bachelor’s degree in a scientific, pharmaceutical, biomedical or related discipline (or equivalent relevant experience). Strong working knowledge of Microsoft Office (Excel, Word, PowerPoint, Outlook and SharePoint). Highly organized with strong attention to detail and the ability to manage multiple priorities in a fast-paced environment. Fluency in English (written and spoken) is required. Fluency in Italian is required. Preferred experience within clinical research, pharmaceutical, or biotech environments, with familiarity in systems such as SAP SuccessFactors, eTMF, DocuSign and Veeva QDocs and an understanding of 21 CFR Part 11. #J-18808-Ljbffr
-
Clinical Trial Associate
19 ore fa
Turbigo, Italia Planet Pharma A tempo pienoPlanet 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 Responsibilities...
-
Global Clinical Trial Ops
17 ore fa
Turbigo, Italia Planet Pharma A tempo pienoA 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...
-
Global Clinical Trial Ops
19 ore fa
Turbigo, Italia Planet Pharma A tempo pienoA 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...
-
Turbigo, Italia Medpace A tempo pienoA 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...
-
Senior Clinical Trial Manager – Remote
2 giorni fa
Turbigo, Italia Syneos Health A tempo pienoA 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...
-
Sr. Clinical Trial Manager
2 giorni fa
Turbigo, Italia Syneos Health A tempo pienoSr. Clinical Trial Manager (Clinical Research Medical Advisor) – FSP – Homebased – ItalyJoin to apply for the Sr. Clinical Trial Manager (Clinical Research Medical Advisor) – FSP – Homebased – Italy role at Syneos Health.Company OverviewSyneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate...
-
Sr. Clinical Trial Manager
2 giorni fa
turbigo, Italia Syneos Health A tempo pienoSr. Clinical Trial Manager (Clinical Research Medical Advisor) – FSP – Homebased – ItalyJoin to apply for the Sr. Clinical Trial Manager (Clinical Research Medical Advisor) – FSP – Homebased – Italy role at Syneos Health.Company OverviewSyneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate...
-
Sr. Clinical Trial Manager
2 giorni fa
Turbigo, Italia Syneos Health A tempo pienoSr. Clinical Trial Manager (Clinical Research Medical Advisor) – FSP – Homebased – Italy Join to apply for the Sr. Clinical Trial Manager (Clinical Research Medical Advisor) – FSP – Homebased – Italy role at Syneos Health. Company Overview Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate...
-
Turbigo, Italia AstraZeneca A tempo pienoA 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...
-
Business Development Associate
2 giorni fa
Turbigo, Italia OPIS A tempo pienoAt OPIS, a leading international Clinical Research Organization (CRO), we are seeking a Business Development Associate who will help expand our global client network across the life sciences sector, focusing on the EU region.You’ll collaborate with senior leaders to identify new business opportunities, research target companies, and connect with key...