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Offerte di Lavoro Clinical Monitor

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1 - 15 di 192
Risultati di Ricerca - Lavoro Clinical Monitor
Parexel International-Firenze
Job Summary: The Site Monitor will be responsible for data integrity, data quality and ensuring compliance with International Council for Harmonization and Good Clinical Practice (ICH GCP) and local requirements at the site level. Monitoring will...
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Barrington James-Italia
technology. Following successful clinical trials, we’re expanding our team to support ongoing and future studies, including international trials. Job Description: We’re looking for a Senior Clinical Research Associate (SCRA) or Senior Field Clinical Trial...
IQVIA Italia-Italia
regulatory requirements. RESPONSIBILITIES:  •  Lead the planning, implementation, and execution of clinical trials, ensuring adherence to timelines, budget, and quality standards.  •  Oversee site selection, recruitment, and monitoring activities for clinical...
Resourcing Life Science-Italia
currently seeking a Clinical Contract Specialist office based in Italy. Job Overview  •  Prepare & negotiate site contracts for the assigned studies  •  Monitor timelines for site contract and budget  •  Point of contact for the Clinical Trial Agreements...
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Barrington James-Casalnuovo di Napoli
technology. Following successful clinical trials, we’re expanding our team to support ongoing and future studies, including international trials. Job Description: We’re looking for a Senior Clinical Research Associate (SCRA) or Senior Field Clinical Trial...
Resourcing Life Science-Italia
Company Description Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are...
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IQVIA Italia-Milano
regulatory requirements. RESPONSIBILITIES:  •  Lead the planning, implementation, and execution of clinical trials, ensuring adherence to timelines, budget, and quality standards.  •  Oversee site selection, recruitment, and monitoring activities for clinical...
Penumbra-Bologna
a clinical resource in the field, supporting the sales team with product expertise and insights.  •  Monitor product performance and case outcomes and provide structured feedback to internal stakeholders.  •  Support and facilitate educational events such as...
OPIS-Italia
The Junior Statistical SAS Programmer, under the supervision of the Direct Manager, is mainly involved in developing SAS programs for the generation of datasets, tables, figures and listings for clinical studies (according to ICH E3), publications...
Resourcing Life Science-Milano
Company Description Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are...
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Akkodis-Italia
Plan [DMP], Prescription Drug Monitoring Program [PDMP], Case Report Form [CRF], Clinical Study Report [CSR])  •  Provide high-quality and timely statistical analyses results to support correct and timely decision making.  •  Act as a statistical...
Alira Health Group-Catania
and functions independently to conduct site monitoring responsibilities for clinical trials; as well as providing oversight, leadership, and guidance in the management and execution of clinical trials to ensure compliance and quality. The Sr CRA works closely...
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OPIS-Maserà di Padova
The Junior Statistical SAS Programmer, under the supervision of the Direct Manager, is mainly involved in developing SAS programs for the generation of datasets, tables, figures and listings for clinical studies (according to ICH E3), publications...
Accelera - Part of NMS Group-Nerviano
About Accelera Accelera is a Preclinical CRO (Contract Research Organization) and offers unparalleled expertise in bringing innovative drug candidates from the Discovery to the Clinical Phases. Over the years, Accelera has brought new products...
Akkodis-Maserà di Padova
Plan [DMP], Prescription Drug Monitoring Program [PDMP], Case Report Form [CRF], Clinical Study Report [CSR]) Provide high-quality and timely statistical analyses results to support correct and timely decision making. Act as a statistical representative...
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