Sr Clinical Data Associate

What You'll Do: Conduct pre-entry review of clinical data Review and issue queries for case report form (CRF) data based on automated edit checks, manual review, and sponsor requirements Assist with set-up of data management study files and the collection,

Job Purpose / Summary This person will serve as the primary CTI Clinical Data Management (CDM) contact with sponsors and represent the DM group on CTI project teams. Responsible for study-specific CDM document development and maintenance, project status to the CTI project team, CDM management, and sponsors. Also, they are responsible for the data cleaning...

JOB PURPOSE / SUMMARY This person will serve as the primary CTI Clinical Data Management (CDM) contact with sponsors and represent the DM group on CTI project teams. Responsible for study-specific CDM document development and maintenance, project status to the CTI project team, CDM management, and sponsors. Also, they are responsible for the data cleaning...

JOB PURPOSE / SUMMARY This person will serve as the primary CTI Clinical Data Management (CDM) contact with sponsors and represent the DM group on CTI project teams. Responsible for study-specific CDM document development and maintenance, project status to the CTI project team, CDM management, and sponsors. Also, they are responsible for the data cleaning...

CTI Clinical Trial and Consulting Services in Portugal is seeking an experienced Clinical Data Manager to support data management activities across clinical studies in a GMP-compliant environment. You will review CRFs, ensure data quality, and maintain essential study documentation. The role involves training CDA staff, refining SOPs, and coordinating with...

CTI Clinical Trial and Consulting Services in Portugal is seeking an experienced Clinical Data Manager to support data management activities across clinical studies in a GMP-compliant environment. You will review CRFs, ensure data quality, and maintain essential study documentation. The role involves training CDA staff, refining SOPs, and coordinating with...

Clinical Research Associate II At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise. As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that...

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise. As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a...

Clinical Research Associate II At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that...