6 Sasstat Jobs

As a Principal Statistical Programmer at AstraZeneca's Alexion division, you will be instrumental in developing and validating programs to create datasets according to Alexion and ADaM specifications. Your expertise will be crucial in analyzing efficacy data through Tables, Listings, and Figures (TLFs) while ensuring compliance with ICH guidelines, Good Clinical Practices, and regulatory requirements. You will also lead programming efforts, represent Clinical and Statistical Programming in meetings with internal and external clients, and mentor other Statistical Programmers in integrating statistical concepts efficiently with SAS Programming. Key Responsibilities: - Develop and validate tech...

You should have 4 to 5 years of experience in SAS/STAT, SAS Data Management, SAS, and Base SAS. As the ideal candidate, you will possess a strong background in Statistical Programming and Biostatistics. Your role will involve leading the team in developing and implementing statistical programming solutions using SAS/STAT, SAS Data Management, and Base SAS. You will also be responsible for overseeing the creation and validation of datasets, tables, listings, and figures for clinical trials. This position requires expertise in Clinical SAS and Power BI within the Pharmaceutical industry. The role falls under the category of Life Sciences and Pharma, and it is a full-time, permanent employment ...

You are a highly skilled Senior SAS Programmer sought to support statistical programming activities for clinical trials. Your responsibilities include end-to-end SAS programming for analysis and reporting, ensuring regulatory compliance, data standards, and high-quality deliverables. Your expertise in efficacy analysis, SDTM and ADaM generation, and TLF programming is crucial for this role. You will manipulate, analyze, and report clinical trial data using SAS, generating and validating SDTM and ADaM datasets in adherence to CDISC standards. Additionally, you will create and validate Tables, Listings, and Figures (TLFs) for study reports and regulatory submissions. Your role involves develop...

The Senior/Principal Clinical Database Manager is responsible for the design, development, testing, implementation, maintenance, and support of clinical databases and applications. You will interface directly with the internal team, EDC vendor, clients, and third-party vendors to gather requirements and provide status updates. Providing operational and technical training to end users and junior staff is a key aspect of this role. Additionally, you may play a lead role in internal software projects that require specialized programming and/or scripting. To be considered for this position, you must have experience in developing and customizing clinical data management databases in a clinical, s...

You will be responsible for providing statistical programming support to clinical trials at Statistics & Data Corporation (SDC), a specialized contract research organization headquartered in Arizona. Since 2005, SDC has been delivering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies. As part of a technology-enabled service offering, you will contribute to both clinical services expertise and technological support required for successful clinical trials. Your primary responsibilities will include performing all statistical programming necessary for clinical trial analysis and reporting. You will apply appropriate statistical methods for da...

As a Statistical Programmer at Statistics & Data Corporation (SDC), a reputable contract research organization based in Arizona, you will be responsible for providing statistical programming support for clinical trials. Your primary role will involve producing statistical analyses, generating and validating analysis datasets, tables, listings, and figures for clinical trials. You will be required to create SDTM mapping and datasets, develop and maintain project files of SAS datasets and SAS code, and support Data Management in various data-related tasks. Additionally, you will act as a liaison between clinical subcommittees and project teams as needed. Your responsibilities will include over...