474 Sas Programming Jobs - Page 11

The Statistical Programming Manager position is a full-time opportunity based in Mumbai, India, within the Biostatistics team. As a Statistical Programming Manager, you will play a crucial role in supporting project teams on programming matters, managing programming staff, ensuring high-quality delivery, providing leadership and training for the Programming group, and leading the development of Programming standards to maximize efficiencies. To qualify for this role, you should hold a Bachelor/Master's degree in statistics, mathematics, health informatics, computer science, or a related field. Additionally, you should have proficiency in SAS programming skills, at least 5 years of clinical p...

The corporate activities are expanding rapidly, and we are currently looking for a full-time, office-based SAS Programmer to join our Biostatistics team in India, Mumbai. As a SAS Programmer, you will collaborate with a team to complete tasks and projects crucial to the company's success. If you are seeking a dynamic career where you can apply your existing skills and further enhance your professional journey, then this role presents an excellent opportunity for you. Your responsibilities in this role will include writing SAS programs to generate analysis datasets, tables, listings, and figures. You will be required to program, validate, and maintain mapped databases using SAS. Additionally,...

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...

Roles and Responsibility Design and develop visual analytics solutions using SAS Visual Analytics. Collaborate with cross-functional teams to identify business requirements and provide data-driven insights. Develop and maintain complex data models and reports. Implement data visualization best practices to create interactive and dynamic dashboards. Work closely with stakeholders to understand their needs and provide tailored solutions. Stay up-to-date with industry trends and emerging technologies in visual analytics. Job Requirements Strong understanding of IT Services & Consulting principles and practices. Proficiency in SAS Visual Analytics and related tools. Excellent communication and p...

- Tasks have been carried out independently and the status is communicated back to all relevant parties. - Ensuring that the electronic data generated is transferred to the customer as per the Data Specifications - Configure, QC, and Test Study EDT and obtain client sign off on approved DTS. - Ensure EDT is delivered in accordance with the required frequency and specifications. - Control the receipt and integration of partner or 3PL data, as per scope of study. - Perform data reconciliations within the context of the assigned team, [and service], as appropriate to ensure a clean data set. - Perform approved data cleaning functions in order to maintain a clean data set. - Adherence to all wri...

We are looking for a skilled SAS Developer with 4 to 6 years of experience in data analytics to join our team at Lericon Informatics Pvt. Ltd. The ideal candidate will have a strong background in IT Services & Consulting, particularly in data analytics and SAS development. Roles and Responsibility Design, develop, and implement data analytics solutions using SAS. Collaborate with cross-functional teams to identify business requirements and develop solutions. Develop and maintain large-scale data systems and databases. Analyze complex data sets to extract insights and trends. Create reports and dashboards to present findings to stakeholders. Troubleshoot and resolve technical issues related t...

Designation: Clinical Data Manager Full Time Opportunity Job Description: - Tasks have been carried out independently and the status is communicated back to all relevant parties. - Ensuring that the electronic data generated is transferred to the customer as per the Data Specifications - Configure, QC, and Test Study EDT and obtain client sign off on approved DTS. - Ensure EDT is delivered in accordance with the required frequency and specifications. - Control the receipt and integration of partner or 3PL data, as per scope of study. - Perform data reconciliations within the context of the assigned team, [and service], as appropriate to ensure a clean data set. - Perform approved data cleani...

Statistics & Data Corporation (SDC) is a specialized contract research organization (CRO) based in Arizona, offering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005. SDC provides technology-enabled services to equip clients with the necessary clinical services expertise and technology for successful clinical trials. As a Statistical Programmer at SDC, your primary responsibility will be to provide statistical programming support for clinical trials. This includes generating and validating analysis datasets, tables, listings, and figures for clinical trials, creating SDTM mapping and datasets, and maintaining the infrastructure ...

The Clinical Database Programmer (CDP) within the Global Clinical Data Management (GCDM) department is responsible for managing Clinical Data Programming activities. Your role involves ensuring the timely creation, validation, testing, implementation, and maintenance of databases required for all assigned projects. You will analyze study protocols and project requirements, identify data quality rules, and design data entry interfaces in compliance with study protocols, Data Management Plans (DMP), Standard Operating Procedures (SOP), and relevant regulatory requirements and standards. You will be responsible for deploying complete, accurate, and efficient clinical study databases to support ...

Veramed prides itself on providing the highest quality statistics and programming consultancy for its clients, and offering its employees an industry-leading working environment with support and training for career growth. We are seeking a hands-on Programmer with attention to detail and a strong work ethic to work as part of the statistical and programming team, providing programming support to a variety of clients in the Veramed portfolio. This role provides the opportunity to progress towards becoming a Lead Programmer at Veramed. This role entails a wide variety of responsibilities and client exposure - you are certainly not pigeonholed. Below is a range of the types of tasks you could b...

At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. We are seeking a skilled SAS Clinical Programmer III with experience in SAS and EDC programming to join our dynamic team. In this role, you will leverage your expertise in SAS programming and clinical data management to support the analysis and reporting of clinical trial data. Your contributions will be pivotal in ensuring the accuracy and integrity of our clinical databases. As a Clinical Programmer III at Allucent, you will lead and coordinate clinical programming activities and ma...

Job Description: Role Title: Senior Analyst - Analytics, Diversified, Value & Lifestyle (L08) Company Overview: Synchrony (NYSE: SYF) is a premier consumer financial services company delivering one of the industry s most complete digitally enabled product suites. Our experience, expertise and scale encompass a broad spectrum of industries including digital, health and wellness, retail, telecommunications, home, auto, outdoors, pet and more. We have recently been ranked #2 among India s Best Companies to Work for by Great Place to Work. We were among the Top 50 India s Best Workplaces in Building a Culture of Innovation by All by GPTW and Top 25 among Best Workplaces in BFSI by GPTW. We have ...

We are hiring for one of our client an IT company based from Ahmedabad,Gujarat Job Title :- SAS Developer Experience: 2 to 5 years Location:- PAN INDIA (willing to relocate) Required Candidate profile SAS Base, Macros, SQL, DI, VA, Viya RDBMS: Oracle, SQL Server, Teradata Data validation, analytics, reporting Banking data models & regulatory reporting SAS Enterprise Guide, AML/KYC

Biostatistician II statistical analyses for clinical research studies as outlined in statistical analysis plans, including creating statistical graphics and verifying randomization codes. They prepare statistical sections of protocols, including sample size calculations, annotate shell data displays, and provide specifications for the structure, content, and algorithms of status and analysis datasets. They perform and oversee quality control (QC) of data displays with inferential statistics. Statisticians report to the Biostatistics Manager. QUALIFICATIONS FOR ESSENTIAL FUNCTIONS Develop, validate, and maintain SAS programs to create analysis datasets, tables, listings, and figures (TLFs) as...

Responsible for the creation, design, analysis and execution of specific projects/analytics for assigned functional area High degree of judgment and independent decision making for complex issues and problem solving Ability to work collaboratively with cross-functional partners to understand and address key business challenges Work independently on analytical tasks starting with problem identification, defining objectives, data discovery and analysis of large & complex data points, formulating concise conclusions with actionable recommendations, creating presentations to pitch findings and strategies Providing clear/concise oral and written communication across various functions and levels, ...

B.Pharmacy Freshers With SAS Training 2023 & 2024 Passouts Only are Eligible Must have Completed SAS Training With good Knowledge in SAS SDTM, Tables & Listing, Adams and Macros. Understanding of relational data base structure & data systems. Required Candidate profile Review protocols for completeness, appropriateness of clinical design and sound statistical analysis. Develop statistical analysis plans, including table, listing and graph specifications.

As a Project Manager, you will be responsible for managing project tasks and ensuring the successful execution and delivery of projects. You will define project deliverables, controls, and supervise the team to ensure adherence to these. Monitoring project progress and ensuring alignment with client expectations will be a key part of your role. Additionally, you will be involved in communications, including deck writing, and coordination of all sub-team efforts. Your responsibilities will also include creating project plans, defining milestones and timelines, and reviewing these plans with the team. Facilitating and gathering client feedback on problem structuring will be crucial. Understand...

You will be a valued member of our clinical research team as a Statistical Programmer, where your primary responsibility will be to program, validate, and deliver statistical outputs for clinical trials. In this role, you will play a crucial part in ensuring compliance with regulatory standards and industry best practices. Your key responsibilities will include developing and maintaining SAS programs for clinical trial data processing, analysis, and reporting. You will be required to map clinical trial data to CDISC standards (SDTM and ADaM) to ensure compliance with regulatory requirements. Creating and maintaining analysis datasets following CDISC implementation guidelines will also be a p...

The Clinical Data Associate II provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. You will follow Standard Operating Procedures / Work Instructions (SOPs/WIs), regulatory directives, study specific plans, and guidelines. Your responsibilities include supporting the Lead DM, performing data entry for paper-CRF studies when necessary, conducting quality control of data entry, developing CRF specifications, assisting in building clinical databases, and maintaining quality controlled database build documentation. You will also specify requirements fo...

Senior Statistical Programmer II (DMC) - Office or Home - India ICON plc is a world-leading healthcare intelligence and clinical research organization. We re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Senior Statistical Programmer I to join our diverse and dynamic team. As a Senior Statistical Programmer I at ICON, you will play a crucial role in analyzing clinical trial data and supporting the statistical analysis process to ensure high-quality results. You will contribute to the success of our clinical studies by developing and validating stat...

Senior Statistical Programmer II (DMC) - Office or Home - India We are currently seeking a Senior Statistical Programmer I to join our diverse and dynamic team. As a Senior Statistical Programmer I at ICON, you will play a crucial role in analyzing clinical trial data and supporting the statistical analysis process to ensure high-quality results. You will contribute to the success of our clinical studies by developing and validating statistical programs, collaborating with biostatisticians, and ensuring compliance with regulatory standards. What You Will Be Doing: Developing and validating SAS programs for statistical analysis and reporting of clinical trial data. Collaborating with biostati...

Create and execute unit/system/integration tests for SAS migration to Viya and Snowflake. Focus on data validation, automation, and code compliance. Preferred candidate profile 5 + years of experience Must to have: SAS programming, SQL, Snowflake, SAS Viya, SonarQube, test automation tools Good to have: Talend, IBM Data Replicator, Qlik Replicate, CI/CD, cloud experience

Job Title: SAS Migration Test Engineers Location: Hyderabad (5 days WFO) Employer: Sonata Software Experience Required: 5+ years in SAS Migration Testing Employment Type: [Full-Time] Key Skills Must have: SAS programming, SQL, Snowflake, SAS Viya, SonarQube, test automation tools Good to have: Talend, IBM Data Replicator, Qlik Replicate, CI/CD, cloud experience Job Description: Create and execute unit/system/integration tests for SAS migration to Viya and Snowflake. Focus on data validation, automation, and code compliance.

Job Summary Synechron is seeking an experienced SAS Developer with a strong focus on production support to join our team. The role involves designing, developing, and maintaining SAS-based analytics solutions while ensuring the stability, performance, and security of SAS applications in a production environment. The ideal candidate will play a key part in supporting data-driven decision-making, troubleshooting issues efficiently, and collaborating across teams to ensure seamless operations that align with organizational goals. Software Requirements Required: SAS Base, SAS Macro, SAS SQL, SAS Enterprise Guide (latest/or recent stable versions) SQL proficiency with relational databases such as...

In this role you will be part of our Centre of Excellence team working specifically in SDTM therefore extensive experience and knowledge is required in this area. What you'll be doing: Develops SAS programs to generate listings, tables and figures as outlined by mock TLF shells Performs quality control (source code review, double-programming and log review) of SAS programs Develops SAS programs to generate CDISC and other analysis data sets as outlined by respective specifications Prepares specifications for CDISC and other analysis data sets Assists Data Management with SAS programming needs Acts as Lead Biostatistical Programmer to interact with the Lead Biostatistician and the study team ...