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...
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...
a Senior Clinical Research Associate / Clinical Research Associate II or Clinical Research Associate I to join our Global ClinicalMonitoring and Site Management team.
You will help biotech, medtech, and specialty pharma companies transform life-changing...
and III
• Start Date: May/June 2025
• Study Duration: 6–12 months (depending on trial progression)
• FTE: 0.5
• Location: Italy
Key Responsibilities:
• Monitorclinical study sites in the cardiology therapeutic area, ensuring compliance with study...
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...
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...
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...
and IIIStart Date: May/June 2025Study Duration: 6–12 months (depending on trial progression)FTE: 0.5 Location: Italy Key Responsibilities: Monitorclinical study sites in the cardiology therapeutic area, ensuring compliance with study protocols, regulatory...
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...
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...
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...
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...
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...
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...
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...