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...
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...
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...
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...
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...
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...
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...
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...
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...
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...
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...
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...
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...