Lavori attuali relativi a Clinical Trial Assistant - Milan - Evidilya


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    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...


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    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...


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  • Milan, Italia PHIDEALIVE Srl A tempo pieno

    Company Description Phidealive, established in 2018, is a Contract Research Organization (CRO) with a strong foundation in Italy’s rich clinical research culture. Positioned as a Clinical Research Atelier, Phidealive emphasizes scientific rigor, regulatory compliance, and a tailored operational approach for each project. The company collaborates with...


  • Milan, Italia PHIDEALIVE Srl A tempo pieno

    Company Description Phidealive, established in 2018, is a Contract Research Organization (CRO) with a strong foundation in Italy’s rich clinical research culture. Positioned as a Clinical Research Atelier, Phidealive emphasizes scientific rigor, regulatory compliance, and a tailored operational approach for each project. The company collaborates with...

Clinical Trial Assistant

2 giorni fa


Milan, Italia Evidilya A tempo pieno

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 the beginning to the end).Prepare, manage, share, and archive the study documents and reports according to protocols, SOPs and applicable regulations.Evaluate the quality and integrity of study site, performing periodical reviews (TMF and TCF)Support CPM and CRA on the development and maintenance of Trial Master File and Trial Center FilesAssist the CPM, tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. Support start-up phase and the on-boarding of the main stakeholders/suppliers.Manage the relationship with the sponsor and update the CPM on the status of the trial.QualificationsMaster's Degree in scientific discipline or health care preferred.Strong organizational and decision-making skillsFluent in EnglishRecruiting start date: September 2025Candidates are invited to send their curriculum vitae and Cover letter authorizing the processing of personal data pursuant to art. 13 of Regulation (EU) no. 2016/679 ("GDPR")