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Senior Statistical Programmer - King Of Prussia Pennsylvania
Company: CSL Behring Location: King Of Prussia, Pennsylvania
Posted On: 01/21/2025
CSL Behring is a global biotechnology leader, guided by a promise to save and improve lives. Millions of people around the world are living with rare and serious medical conditions. CSL Behring is committed to delivering medicines that improve their lives.With operations in 35+ nations and 30,000 employees worldwide, CSL is inspired to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment. CSL is the parent company of CSL Behring, CSL Plasma, CSL Seqirus and CSL Vifor. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions.Could you be our next Senior Statistical Programmer The job is located in the King of Prussia office. This is a hybrid position. You will report to the Associate Director of Statistical Programming.You will provide hands-on support and technical guidance on clinical study teams. You will develop study and ad hoc output including: ADaM datasets, tables, figures and listings output and QC of requested output is the main focus of this role. You will work with the study statistician will be responsible for review and acceptance of contract research organization (CRO) deliverables which are datasets in submission ready standard format (ADaM), tables, figures and listings and submission packages. You will participate in the design and quality control process for SAS programs used to access, extract, transform, review and submit clinical data for all requested analyses. You will partner with other departments (eg, Biostatistics, Data Management, Regulatory Operations, Medical Writing, ESP teams) to ensure Standard Operating Procedures are followed and the correct study data are used for all requests. You will participate in department and technology development and process improvement programsResponsibilities: - Collaborate with peers and statisticians to ensure the quality and accuracy -thus submission readiness -of clinical data by authorities (i.e. SDTM, ADaM, tables, figures, listings, and define.xml).
- Lead requested efforts for pooled and exploratory analyses working with clinical programming team and their collection of legacy data.
- Lead the in-house specification and delivery of ISS and ISE datasets and associated output (tables, figures, and listings) when not provided by CRO.
- Lead the design and implementation of complex SAS programs for applications designed to report complex clinical trial data in CDISC ADaM format.
- Identify problems and develop global tools that increase the efficiency and capacity of the Statistical Programming group.
- Perform additional statistical analyses including: support responses to regulatory agencies, create integrated summary of safety and efficacy, support publications and presentations, support reporting of clinical trials with exploratory analyses of available data, replicate CRO and CSL statistician analyses for QCQualifications:
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