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...
Per la sede italiana (provincia di Milano) di un’importante CRO, ricerchiamo Clinical Research Associate (CRA).
Previsto un inserimento diretto in azienda, a tempo indeterminato.
Inquadramento e retribuzione saranno parametrati sull’esperienza...
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...
Pls note: Incumbent can be based anywhere in Europe or the US.
Role Overview:
This position is intended to head and support the clinical development of new drugs conception of innovative approaches to plan clinical studies and support end to end...
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...
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 and thrive under demanding...
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...
and collaborators based in Italy, supporting clinical development. External vendors include CROs, CMOs, central labs and bioanalytical labs. External collaborators include academic and clinical researchers. This role works cross-functionally with internal...
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 within cross...
Evidilya, the dedicated Contract Research Organization of Sprim Health Group operates as a full-service international expertise in successfully developing and managing observational, pre-clinical and clinical trials, is looking for a:
Business...
and collaborators based in Italy, supporting clinical development. External vendors include CROs, CMOs, central labs and bioanalytical labs. External collaborators include academic and clinical researchers. This role works cross-functionally with internal...
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...
Functions:
1. Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization...