5 Sasstat Jobs

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 opportunity. Key Skills: - Clinical SAS - Power BI If you are interested in this position, please refer to the following details: Job Code: GO/JC/21042/2025 Recruiter Name: HariharanA,

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 developing complex ad-hoc reports from raw clinical data and applying a deep understanding of efficacy analyses and clinical endpoints. Contribution to the preparation and review of submission documents and eCRTs is expected, as well as production programming and quality control to ensure accuracy and consistency. As a team player, you will commit to quality and meeting project deadlines, remaining adaptable and flexible in a fast-paced clinical environment. Qualifications required include a Bachelors or Masters degree in Life Sciences, Statistics, Computer Science, or a related field, along with 6+ years of hands-on experience in clinical trial programming using SAS. Proficiency in CDISC standards, Base SAS, SAS Macros, SAS/STAT, and SAS/GRAPH is essential. Experience in generating datasets and outputs for regulatory submissions and familiarity with eCTD standards are preferred. Strong attention to detail and analytical problem-solving skills are necessary for this role. Join a collaborative team environment where your expertise in clinical data programming directly contributes to advancing global healthcare. Precision, integrity, and innovation are valued in every project undertaken.,

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, scientific, or health care discipline. A combination of related experience and a Bachelor's degree is required. You should also be a Medidata Rave EDC Certified Study Builder with experience in Rave API integration and Advanced Custom Function programming. Proficiency in Microsoft Office applications, handling various clinical research tasks, excellent organizational and communication skills, and a professional command of the English language are essential for this role. Experience in Object-Oriented Programming, scripting languages, SAS, R, SQL, CDISC standards, and clinical database management systems is also necessary. Broad knowledge of drug, device, and/or biologic development, effective data management practices, strong leadership, and interpersonal skills are key qualifications. Preferred qualifications include experience in Oncology and/or Orphan Drug therapeutic areas, proficiency in Base SAS, SAS/STAT, SAS/ACCESS software, SAS Macro programming language, advanced database management experience, and Veeva set-up experience. If you require a reasonable accommodation to complete the application process or need an alternative method for applying due to a disability, please contact Precision Medicine Group. Please be aware of potential fraudulent employment offers and note that our organization follows a formal interview process before extending any job offers.,

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 data analysis, review Statistical Analysis Plans, and design/develop SAS macros and utilities to streamline programming activities. Additionally, you will generate tables, listings, and figures per protocol and client requests, participate in program validation and quality control activities, and develop SDTM and ADaM datasets. You will collaborate with various departments such as Clinical Operations, Project Management, and Data Management to ensure high client satisfaction through successful project execution. Your role will also involve mentoring junior statistical programmers, maintaining project files, adhering to quality systems, and complying with data integrity and business ethics requirements. To be successful in this role, you must possess strong analytical skills, proficiency in SAS programming (including SAS/Base, SAS/Stat, and SAS Macros), and a basic understanding of SAS/Graph. You should have a solid grasp of statistical programming, the ability to identify and resolve data issues, and excellent communication skills to convey technical concepts clearly to non-statistical colleagues. Familiarity with clinical trial design, regulatory guidelines, and CDISC SDTM and ADaM data models is essential. Ideally, you should hold a Bachelor's degree in computer science, statistics, or a related scientific field, along with four years of relevant professional experience. SDC offers a supportive work environment that values employee development, growth opportunities, career advancement, flexible work schedules, an engaging culture, and various benefits. Join SDC's dynamic team and contribute to the successful execution of client clinical programs while being part of a company that fosters innovation, growth, and a sense of belonging among its employees.,

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 overseeing statistical programming activities for medium to large-scale projects, applying appropriate statistical methods for data analysis, and providing statistical programming expertise to project teams. You will review the Statistical Analysis Plan, lead the development of SAS macros and utilities, and conduct internal training sessions. Furthermore, you will be responsible for generating tables, listings, and figures as per protocol requirements, participating in statistical program validation activities, and developing SDTM and ADaM datasets. You will also ensure compliance with CDISC and FDA guidelines, develop define.xml and study data reviewer's guides, and communicate effectively with project teams and management. In addition to the technical aspects of the role, you will play a key role in mentoring junior statistical programmers, managing programming timelines and budgets, and ensuring adherence to SDC's standard procedures and quality system. Strong analytical and problem-solving skills, proficiency in SAS programming, and knowledge of regulatory guidelines are essential for this position. To qualify for this role, you should possess a Bachelor's degree in computer science, statistics, or a related scientific field, along with at least six years of relevant professional experience. Certification in SAS Base, Advance, and Clinical Trials is preferred. At SDC, we are committed to the growth and development of our employees, providing a flexible work schedule, engaging work culture, and career advancement opportunities. Our company culture is centered around core values such as Energy, Integrity, Engagement, and Innovation. Join our team and be part of a dynamic and innovative organization that is dedicated to supporting both our clients and employees in this ever-evolving industry.,