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Offerte di Lavoro Clinical Monitor

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1 - 15 di 159
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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CliniRx-Italia
in a scientific discipline.  •  Experience: 1-4 years of experience in site monitoring within clinical research.  •  Skills: Strong understanding of ICH GCP and applicable clinical trial regulations; excellent verbal and written communication; ability to multitask...
44.01 Premier Research S.R.L.-Italia
a Senior Clinical Research Associate / Clinical Research Associate II or Clinical Research Associate I to join our Global Clinical Monitoring and Site Management team. You will help biotech, medtech, and specialty pharma companies transform life-changing...
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Upsilon Global-Italia
and III  •  Start Date: May/June 2025  •  Study Duration: 6–12 months (depending on trial progression)  •  FTE: 0.5  •  Location: Italy Key Responsibilities:  •  Monitor clinical study sites in the cardiology therapeutic area, ensuring compliance with study...
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-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...
Upsilon Global-Italia
and IIIStart Date: May/June 2025Study Duration: 6–12 months (depending on trial progression)FTE: 0.5 Location: Italy Key Responsibilities: Monitor clinical study sites in the cardiology therapeutic area, ensuring compliance with study protocols, regulatory...
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Barrington James-Roma
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-Brescia
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...
Barrington James-Roma
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-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...
CliniRx-Roma
in a scientific discipline.  •  Experience: 1-4 years of experience in site monitoring within clinical research.  •  Skills: Strong understanding of ICH GCP and applicable clinical trial regulations; excellent verbal and written communication; ability to multitask...
IQVIA Italia-Bergamo
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...
Skills Alliance-Italia
Job Description:The position includes a diverse set of duties. In addition to your critical role in overseeing and managing clinical trials, you will take on advanced proctoring responsibilitiesAs a Clinical Specialist, you will train study site...
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