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
(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
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
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
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
development and coordination of Reports & Dashboards using tools such as Power BI, SAP SAC, AfO, and othersFacilitate effective requirement management, ensuring clear communication and alignment across diverse
development and coordination of Reports & Dashboards using tools such as Power BI, SAP SAC, AfO, and othersFacilitate effective requirement management, ensuring clear communication and alignment across diverse
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
development tests in alignment with test management and developers Analysis of results and creation of structured test reports Analyze, document, report and follow up on issues using a defect management system
development tests in alignment with test management and developers Analysis of results and creation of structured test reports Analyze, document, report and follow up on issues using a defect management system
in business development activities for target clients and contribute to advancing JLL's market position in sustainability.Regularly report on progress to the Head of Sustainability - EMEA Markets Advisory and
site meets all financial targets and control requirements Provide standard monthly/quarterly/annual reporting and management reports as required Deliver Savings within or above the given targets
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
/ savings from tenders / process re-design / negotiation initiatives and provide monthly/ Quarterly reports to Sourcing & Procurement LeadershipTo ensure that all vendor details and files are complete and