via regular tracking KPI reports • Manage end to end query resolution process, managing cross functional stakeholders to ensure a full and timely response is provided • Provide additional insights
Conference on Harmonization (ICH) guidelinesManaging progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolutionCollaborating with experts at study
regulatory submissions, recruitment, case report form (CRF) completion, and data query resolutionCollaborating with experts at study sites and with client representativesDepending on client model there might
statistical reports. Requirements: BSc or MSc degree in Biostatistics or related field and between 5-7 years’ relevant experience within the life-science industry, along with at least 1-year experience
regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.Managing progress by tracking regulatory submissions, recruitment, case report form
Conference on Harmonization (ICH) guidelines.Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution.Collaborating with experts at study
ensure that target enrollment will be met across the allocated countries.Drive study compliance by maintaining and updating trial management systems, using study tools and management reports available to
IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory