... on other functional plans (eg. Data Management Plan, Communication Plan) as they relate to the clinical trial management activities. • Responsible for development and ongoing maintenance of clinical study tools and templates, including ...
... -technical stakeholders. Strong understanding of clinical trial processes, regulatory requirements, and best practices in data management and analysis. What ICON can ...
... Monitoring management team. The Lead CRA ensures the monitoring activities of their assigned study(s) are in accordance with sponsor policies and procedures, ICH GCP and local regulations. The LCRA will report directly to the Associate Director, Clinical ...
... for clinical trials Ensure all systems both ... dependencies between Data Operation stakeholders (Data Management, Programming, Biostatistics) either within Parexel or at a client Work with study teams and Data Standards Associates to ensure enforce the use ...
... safety and clinical data integrity at an investigator physician site such as protocol deviation violations and pharmacovigilance issues. Per the Clinical Monitoring Site Management Plan (CMP SMP): Assesses ... risks associated with blinded or randomized information ...
... safety and clinical data integrity at an investigator physician site such as protocol deviation violations and pharmacovigilance issues. Per the Clinical Monitoring Site Management Plan (CMP SMP): Assesses ... risks associated with blinded or randomized information ...
... safety and clinical data integrity at an investigator physician site such as protocol deviation violations and pharmacovigilance issues. Per the Clinical Monitoring Site Management Plan (CMP SMP): Assesses ... risks associated with blinded or randomized information ...
... safety and clinical data integrity at an investigator physician site such as protocol deviation violations and pharmacovigilance issues. Per the Clinical Monitoring Site Management Plan (CMP SMP): Assesses ... risks associated with blinded or randomized information ...
... Trial Management System application for clinical study execution and reporting. Ensure the clinical studies are conducted according to procedures including up to date and complete trial master files, regular review of data, and assurance that monitoring ...
... lot of perks Job Title: Data Engineer Location: Newcastle (Hybrid Working) ... and maintain the integrity of data assets. Key Requirements: Proven experience with data storage, data integration, and data analytics technologies (e.g., SQL ...