Clinical Research Associate: Site Monitoring & Study Delivery
IQVIA Argentina
pIQVIA is seeking a Clinical Research Associate to perform site monitoring visits and ensure studies are conducted per protocol and regulations. You will manage site communications, training, and documentation. /ppYou will track recruitment, CRF completion, data queries, and regulatory submissions, and support start-up and TMF/ISF maintenance. Strong English and MS Office skills are expected; some site financial tasks may be required. /p #J-18808-Ljbffr
Offerta di lavoro pubblicata 2 giorni fa
Offerte di lavoro simili
33.900 € - 61.700 €
...Overview Perform monitoring and site management work to ensure... ...are conducting the study(ies) and reporting... ...requirements, i.e., Good Clinical Practice (GCP) and... ...progress of assigned studies by tracking regulatory... ...applicable clinical research regulatory requirements...ConsigliatoPart-timeTempo pienoDisponibilità immediata- ...Overview In this role you support multicenter clinical studies by monitoring sites to ensure protocol adherence and data reporting per GCP/ICH guidelines. You will drive site communication, training, and recruitment alignment to project needs, and manage study progress...Consigliato
55.000 € - 65.000 €
...passionate about oncology research and looking to join a... ...(TRIO) is a global clinical research organization dedicated... ...Clinical Research Associate to join our Monitoring Resources team. Reporting... ...: Conducting site visits, including pre-study, initiation, monitoring...ConsigliatoTempo pienoLavoro da casaOrario flessibile44.800 €
...ul liThe CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance... ...Manager to ensure study timelines are adhered... ...to ensure timely delivery of study milestones (i... ...knowledge of ICH and associated regulatory guidelines...Consigliato- ...Clinical Research Associate, Sponsor Dedicated – Italy Join to apply for the Clinical Research... ...Responsibilities Performing site selection, initiation, monitoring and close‑out visits... ...Collaborating with experts at study sites and with client representatives...ConsigliatoTempo pienoAuto aziendaleOrario flessibile
- ...Linical Milano (Italy) is seeking a Clinical Research Associate II to oversee multiple investigative sites across Italy. This on-site... ...trials are conducted per study protocols, ICH-GCP, and regulatory... ...clinical research and 2 years monitoring experience, and fluency in...Lavoro da casa
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47.800 € - 63.000 €
...Job Overview Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor,... ...careful source document review. Monitor data for missing or implausible...Part-timeTempo pieno- ...designing and analyzing clinical trials, ensuring data... ...investigators and site staff. You’ll work cross-functionally to monitor trials, resolve data queries... ..., and prepare key study documents. This role sits... ...as a Clinical Research Associate In-depth knowledge...
- ...main CTI contact for assigned study sites /liliConduct site visits (... ...site initiation (SIV), interim monitoring (IMV), and close-out (COV))... ...updates of site status to Clinical Project Manager /liliConduct... .../h3ulli3 - 5 years clinical research experience as a CRA /liliLife...Lavoro ibridoRemoto
40.944 € - 51.180 €
...will design and analyse clinical trials, interpreting... ...contribute to clinical trial monitoring activities, taking... ...Include Conducting site qualification,... ...to facilitate smooth study conduct. Performing... ...experience as a Clinical Research Associate after being certified...- ...Overview In this full-time role, you join Medpace's Clinical Monitoring team to support site-based trials in Italy, helping advance clinical... ...directly impact trial quality, patient safety, and timely study delivery. Retribuzione / Benefits Flexible work...Tempo pienoOrario flessibile
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47.800 € - 63.000 €
ppbJob Overview: /b /p pThe Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or... ...job. /p /li lipServe as lead monitor for a protocol or project and may...Part-timeTempo pieno- ...Overview In this role, you will support multinational clinical studies by coordinating site activities and ensuring high-quality data. You will work within a cross-functional team to monitor sites, manage regulatory submissions, and help optimize recruitment. You'll...Auto aziendaleOrario flessibile
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- ...role, you will lead site management and monitoring for assigned trials... ...functional teams to keep study activities on track... ...lock. You will monitor AEs/SAEs and support... ...contribute to meaningful clinical development across... ...in clinical research ( Oncology preferred...Remoto
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...Clinical Research Associate At ICON Strategic Solutions, you will work in a sponsor... ...to clinical trial monitoring activities, taking responsibility... ...include: Conducting site qualification, initiation,... ...staff to facilitate smooth study conduct. Performing data...Lavoro da remoto- ...Overview In this role you join Medpace's Clinical Monitoring team in Italy to perform site-based monitoring activities for clinical studies. You will receive comprehensive training... ..., monitoring and closeout visits at research sites per protocol Communicate with site...RemotoLavoro da casaOrario flessibile
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- pBeOne Medicine is seeking an experienced Clinical Research Associate to monitor oncology/hematology trials across sites. You will perform feasibility, site selection, and monitoring visits in line with ICH-GCP and internal SOPs, ensuring data quality and safety. /ppCollaboration...
- ...BeOne Medicines in Milano, Italy seeks an experienced Clinical Research Associate to monitor oncology trials across sites, ensuring adherence to ICH-GCP, local regs, and BeOne SOPs. You will perform feasibility and site identification, initiate and conduct visits, and...
- ...In this role you oversee clinical trial monitoring to ensure adherence to protocol... .... You will lead site visits, collaborate with cross... ...pathways Responsabilità Monitor trial sites for protocol... ...experience as a Clinical Research Associate with strong understanding...
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- ...is searching for a Clinical Supply Chain to... ...and US): depot-to-site and site-to-site shipments... ...: inventory monitoring, expiry/lot management... ...a global study supply operation)... ...proven high-quality delivery and results across... ...Trials, CRO, Clinical Research Organization, Clinical...TemporaneoLavoro ibridoRemoto
28.000 € - 34.000 €
...., che Progetta e conduce studi interventistici e Real-World... .../ppbr/ppstrongIn-House Clinical Research Associate /strong /ppbr/ppche guidi... ...studi condotti in remote monitoring/on-site monitoring,. /ppbr/ppstrongPrincipali... ...di CRA / monitoraggio clinico. /liliEsperienza pratica...Libero professionistaContratto con partita IVALavoro ibridoRemoto