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
tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution. Applicants should have: A university degree in a health care or other scientific discipline or a
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
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
electronic Case Report Forms (eCRF) in the eCRF system and associated documentation. Support the development of unique eCRF forms for new studies to ensure their compliance with the CDISC clinical data
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
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
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
(derived datasets) and transfer files for internal and external clients - The programming quality control checks for the source data and to report the data issues periodically • Ability to interpret project