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Job Description & How to Apply Below
Key Responsibilities
• You will program and validate the output (tables, listings and figures) to support the data cleaning and the statistical analyses required for clinical studies, publications, Regulatory and Market Access requests
• You will supervise the generation of the SDTM/ADaM datasets and related documents in compliance with CDISC guidelines as well as the output prepared by the CRO.
• You will develop standard SAS macros, templates and utilities and prepare the corresponding validation documents
• You will interact with the Statistician to prepare tables and listings according with the specification documents
• You will interact with the Data Manager in cleaning activities, external data management and reporting.
• You will interact with the Drug Safety Unit to evaluate the data from the pharmacovigilance database.
• You will lead efforts in the development, maintenance and adherence to divisional SOPs and guidelines.
Required Education Scientific degree (Statistics, Mathematics, Informatics) Required Skills and Experience3-5 years of experience in a CRO or pharmaceutical company and clinical trials.
You have a clear understanding of theoretical and applied statistic and regulatory guidelines in a pharmaceutical research setting; you are expert in the development and submission of NDATechnical Competencies You have knowledge of CDISC standards and preferably GCP.You know programming in SAS System. Optional R and/or SQLRequired Behaviours and Competencies You are collaborative, good communicator and able to interact with all levels of the organization.
Required Languages Fluent in English
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