... oversight dashboards and other clinical trial systems (e.g. Clinical Trial Management System (CTMS), Electronic Data ... QA). Supports Inspection Readiness for clinical trial management scope. • Oversees CRAs and Central Monitors assigned to the study and ...
... inquiries, particularly those related to clinical trial design rationale, from PIs study ... for actively enrolling or planned clinical trials and build relationships with them ( ... awareness about our Client, our clinical trials, our commitment to improving the ...
... all study activities following Good Clinical Practices (GCP). Manage multiple clinical trials simultaneously. Protect the safety of human subjects. Monitor appropriate sources for specific clinical study or federal regulation updates. ...
... Responsibilities: Clinical Trial Monitoring: Conduct site initiation, routine monitoring, and close-out visits to ensure protocol compliance and data integrity. Perform source document verification, review of case report forms, and data validation. Monitor ...
... ; Minimum of 2 years of Clinical Trial Management experience, CRO experience preferred; 5+ years of Project Manager Clinical Trial Manager experience at a CRO ...
... ; Minimum of 2 years of Clinical Trial Management experience, CRO experience preferred; 5+ years of Project Manager Clinical Trial Manager experience at a CRO ...
As a Clinical Trial Delivery Lead, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare ... regulations) You are a Global Clinical Trial Manager with experience in Recruitment ...
... ICH GCP, the conduct of clinical trials and governing regulations, relevant ICON ... • *To assist project teams with trial progress tracking by updating the Clinical Trial Management systems, providing access to ...
... want to be the Clinical Research Organisation that delivers excellence ... an industry. The role: The Clinical Trial Manager is responsible for the delivery of all clinical aspects of the study. The CTM oversees the clinical portion of the budget, develops ...
... pharmacovigilance issues. • Per the Clinical Monitoring Site Management Plan (CMP ... records o Verifies required clinical data entered in the case ... the ISF with the Trial Master File (TMF). Ensures the ... Sites and 675,000+ Trial patients. No matter what your ...