Clinical Trial Assistant
Evidilya
pstrongEvidilya /strong, la Contract Research Organization dedicata di Sprim Health Group, opera come realtà full-service con competenza internazionale nello sviluppo e nella gestione di studi osservazionali, pre-clinici e clinici, ricerca un/una: /ppbr / /ppstrongClinical Trial Assistant (STAGE) /strong /ppper rafforzare il nostro Team Operativo di Milano. /ppbr / /ppstrongAttività principali: /strong /pulliCollaborare e supportare i membri dello study team nell'esecuzione dei progetti (dall'inizio alla fine). /liliPreparare, gestire, condividere e archiviare i documenti e i report di studio in conformità ai protocolli, alle SOP e alle normative applicabili. /liliValutare la qualità e l'integrità del centro di studio, effettuando revisioni periodiche (TMF e TCF). /liliSupportare CPM e CRA nello sviluppo e nel mantenimento del Trial Master File e dei Trial Center Files. /liliAssistere il CPM nel monitoraggio delle sottomissioni e approvazioni regolatorie, del reclutamento e dell'arruolamento, della compilazione e trasmissione delle Case Report Form (CRF), nonché della generazione e risoluzione delle data query. Supportare la fase di start-up e l'on-boarding dei principali stakeholder/fornitori. /liliGestire la relazione con lo sponsor e aggiornare il CPM sullo stato dello studio. /li /ulpbr / /ppstrongRequisiti /strong /pulliLaurea magistrale in discipline scientifiche o sanitarie (preferibile). /liliSpiccate capacità organizzative e decisionali. /liliOttima conoscenza della lingua inglese. /li /ulpbr / /ppstrongInizio selezione: /strong Settembre 2026 /ppCompenso: 800 euro netti mensili /ppbr / /ppI candidati sono invitati a inviare il proprio curriculum vitae e la lettera di presentazione, autorizzando il trattamento dei dati personali ai sensi dell'art. 13 del Regolamento (UE) n. 2016/679 ("GDPR"). /ppbr / /ppemL'annuncio è rivolto a candidati di entrambi i sessi, ai sensi della normativa vigente in materia di parità di trattamento (L. 903/77 e D.Lgs. 198/2006). /em /p
36.640 € - 53.130 €
ph3Clinical Trial Administrator /h3Salary : p€36,640 - 53,130 yearly /p pAzienda : Novo Nordisk Tipo Lavoro : Full Time Italy /p h3Descrizione Lavoro - Clinical Trial Administrator /h3 pClinical Trial Administrator (Fixed Term, One Year Contract) /p pResearch Development...ConsigliatoTempo pienoStage/TirocinioTempo determinato- ...Studi Magna Graecia di Catanzaro in Catanzaro, Italy, seeks a Clinical Research Coordinator and Biomedical Equipment Manager in the Department... ...will oversee biomedical instrumentation, support clinical trial data collection, processing and management, and handle supplier...ConsigliatoTempo determinato
- pMerck Kgaa in Italy is seeking a Clinical Pathology Research Associate to generate high-quality clinical pathology data supporting safety assessment of preclinical drug candidates. You will perform hematology, clinical chemistry, coagulation, urinalysis, and immune phenotyping...Consigliato
- ...quality and excellence. /p pWe are Worldwide Clinical Trials, and we are a global team of over 3,500+... ...or electronic data capture systems and assist sites with data query resolution. /li... ...related documentation for filing in the Trial Master File (TMF). /li liEnsure site...Consigliato
- pWorldwide Clinical Trials in Italy is seeking a Clinical Research Associate (CRA) to work with brilliant minds across Oncology, Neuroscience, Cardiovascular, Metabolic and Rare Diseases. You will support sites, ensure protocol adherence, and contribute to TMF management...Consigliato
- pICON Strategic Solutions is seeking a Senior Clinical Research Associate (CRA) to oversee clinical trial activities in Italy. The role involves monitoring trial... ...competitive salary, health insurance, and assistance programs to support work-life balance. /p #J-18808...
- ...storage, dispensation and accountability of all Investigational Product (IP) and trial-related materials /li liPerform site management activities and provide ongoing updates of site status to Clinical Project Manager /li liConduct remote monitoring and complete related...Lavoro ibridoRemoto
- ...world-leading healthcare intelligence and clinical research organization. We’re proud to... ...role in overseeing and managing clinical trial activities to ensure they are conducted... ...maximize savings. /liliGlobal Employee Assistance Programme, LifeWorks, offering 24-hour access...
- pMedpace seeks full-time Clinical Research Associates for Italy, offering home or office-based work with substantial national travel (60-80%). The role supports the Clinical Monitoring team, performing site visits, data verification, and regulatory review to ensure protocol...Tempo pienoLavoro ibridoLavoro da casa
32.980 € - 38.000 €
...presenting great opportunities for personal development and career advancement across the globe. /ppbYour Role /b /ppYou will join the Clinical Pathology Laboratory within the Development Chemical and Preclinical Safety organization as a motivated Research Associate. In...Tempo pienoStage/TirocinioOrario flessibile- ...the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study... ...liliManage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation...Remoto
28.000 € - 34.000 €
.../ /ppricerca /ppbr / /ppstrongIn-House Clinical Research Associate /strong /ppbr / /ppche... ...con Project Manager e Clinical Trial Assistants. /li /ulpbr / /ppbr / /ppstrongRequisiti... ...documentata in ruoli di CRA / monitoraggio clinico. /liliEsperienza pratica in: PQV, SIV,...Libero professionistaContratto con partita IVALavoro ibridoRemoto- pWorldwide Clinical Trials is seeking a seasoned Clinical Research Associate to work across diverse therapeutic areas including Neuroscience, Oncology, and Cardiovascular. You will monitor sites, ensure protocol adherence, and support TMF processes while collaborating with...
- ...site management and monitoring for assigned trials to ensure patient safety and high-quality... ...the chance to contribute to meaningful clinical development across therapeutic areas.... ...qualification Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local...Remoto
43.000 €
ppOur clinical activities are growing rapidly, and we are currently seeking full-time, home or office-based Clinical Research Associates to join our Clinical Monitoring team in Italy. This position will work with a team to accomplish tasks and projects that are instrumental...Tempo pienoLavoro da casaOrario flessibile- pCTI Clinical Trial and Consulting Services in Italy seeks a Clinical Research Associate to serve as main CTI contact for assigned study sites and to conduct monitoring visits in line with ICH-GCP. You will support start-up activities, manage essential regulatory documents...