03.06.2024 | Full-time | PharmiwebDescription Central Monitor ( Remote Monitor/Risk-Based Monitor) - Romania Sponsor Dedicated The purpose of the Remote Monitor is to de-risk studies as early as possible by analyzing data at the macro-level for insights that are not visible when monitoring individual data points /study sites
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebJob Overview The purpose of the Central Monitor is to de-risk studies as early as possible by analyzing data at the macro-level for insights that are not visible when monitoring individual data points /study sites-thereby enabling sponsor to take early interventions to mitigate potential risks
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebOf therapeutic areas, and build a meaningful, strong career within our organization. Your responsibilities will include Performing site selection, initiation, monitoring and close-out visits Supporting the development of a subject recruitment plan Evaluating the quality and integrity of site practices
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebIs a client dedicated one where you will be monitoring studies in such therapeutic areas as immunology, pulmonology, oncology, cardiovascular or neroscience. The CRA is responsible for the initiation, monitoring and closure of assigned sites in clinical studies, in compliance with sponsor's procedural
Uita-te mai târziu03.06.2024 | Full-time | Cluj-Napoca | PharmiwebYou’ll do Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports. Build relationships. Oversee integrity of the study and utilize problem-solving skills
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebEstablished data review guidelines on Fortrea or client data management systems Requirements Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines Excellent understanding of Serious Adverse Event (SAE) reporting Ability to resolve project
Uita-te mai târziu03.06.2024 | Full-time | Oradea | PharmiwebAnd ensuring study training compliance is maintained Oversees, manages and coordinates monitoring activities from site activation through to study closure at country and site level in accordance with the Monitoring Plans. Reviews monitoring visit reports and metrics, including protocol deviations and follow-up
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebEstablished data review guidelines on Fortrea or client data management systems Requirements Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines Excellent understanding of Serious Adverse Event (SAE) reporting Ability to resolve project
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebYou’ll do Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports. Build relationships. Oversee integrity of the study and utilize problem-solving skills
Uita-te mai târziu03.06.2024 | Full-time | Oradea | PharmiwebIs a client dedicated one where you will be monitoring studies in such therapeutic areas as immunology, pulmonology, oncology, cardiovascular or neroscience. The CRA is responsible for the initiation, monitoring and closure of assigned sites in clinical studies, in compliance with sponsor's procedural
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