474 Sas Programming Jobs - Page 14

:. Soul AI is a pioneering company founded by IIT Bombay and IIM Ahmedabad alumni, with a strong founding team from IITs, NITs, and BITS. We specialize in delivering high-quality human-curated data, AI-first scaled operations services, and more. . We are looking for a skilled Statistical Programmer with at least 2 years of experience to write code for the collection, analysis, and presentation of data in various research and business projects. Key Responsibilities:. Write and optimize statistical code for data analysis and model development. Implement statistical methods for clinical trials, research, and business insights. Work with large datasets, ensuring the data is accurate, clean, and ...

:. Soul AI is a pioneering company founded by IIT Bombay and IIM Ahmedabad alumni, with a strong founding team from IITs, NITs, and BITS. We specialize in delivering high-quality human-curated data, AI-first scaled operations services, and more. . We are looking for a skilled Statistical Programmer with at least 2 years of experience to write code for the collection, analysis, and presentation of data in various research and business projects. Key Responsibilities:. Write and optimize statistical code for data analysis and model development. Implement statistical methods for clinical trials, research, and business insights. Work with large datasets, ensuring the data is accurate, clean, and ...

Overview: We are seeking a highly skilled SAS Administrator to join our team. The SAS Administrator will be responsible for the installation, configuration, maintenance, and support of SAS (Statistical Analysis System) software environments. This role requires a detail-oriented professional with strong technical expertise in SAS and a deep understanding of system performance optimization and data security. Key Responsibilities: Install, configure, and maintain SAS software, including SAS servers, clients, and third-party components. Configure and manage SAS metadata, user permissions, and authentication protocols. Monitor and optimize system performance, ensuring high availability and reliab...

Job Summary: We are seeking a highly motivated and experienced SAS Governance and Compliance Consultant to join our team. In this role, you will be responsible for ensuring the effective implementation and ongoing management of our SAS environment using SAS Governance and Compliance (SAS GRC). You will play a key role in mitigating risks, maintaining compliance with regulations, and promoting best practices for data governance. Responsibilities: Develop and implement data governance policies and procedures to ensure data quality, integrity, and security. Create and enforce guidelines for data management and compliance with regulatory requirements. Monitor and ensure adherence to compliance s...

Role Purpose The purpose of this role is to design, test and maintain software programs for operating systems or applications which needs to be deployed at a client end and ensure its meet 100% quality assurance parameters Do 1. Instrumental in understanding the requirements and design of the product/ software Develop software solutions by studying information needs, studying systems flow, data usage and work processes Investigating problem areas followed by the software development life cycle Facilitate root cause analysis of the system issues and problem statement Identify ideas to improve system performance and impact availability Analyze client requirements and convert requirements to fe...

Select how often (in days) to receive an alert: Select how often (in days) to receive an alert: R&D Programmer III Jun 24, 2025 Bangalore, India, 560064 Who we are The opportunity The Senior Clinical Programmer is responsible to provide high level skills of clinical programming support of clinical projects and regulatory submissions. The Senior Clinical Programmer is playing a lead role generating and validating analysis datasets, tables, listings and figures. The Senior Clinical Programmer participates in the development of global data standards, SDTM, ADaM and Teva s database structure. The Senior Clinical Programmer is responsible for providing professional expertise and leadership throug...

Lead clinical trial statistics: develop protocols, design studies, create TLGs, review ADaM specs. Manage statistical deliverables, mentor team, collaborate cross-functionally. Support CTR prep, regulatory submissions, QC validation. Required Candidate profile Postgrad/PhD Statistics. 3+ yrs clinical trial biostatistics experience. Expertise in protocol design & statistical programming (SAS/R). Regulatory submission knowledge. Team leadership abilities.

Project Role : Application Developer Project Role Description : Design, build and configure applications to meet business process and application requirements. Must have skills : SAS BI Good to have skills : NAMinimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Developer, you will design, build, and configure applications to meet business process and application requirements. Your day will involve collaborating with teams to develop innovative solutions and contribute to key decisions in the project. Roles & Responsibilities:- Expected to be an SME- Collaborate and manage the team to perform- Responsible for team dec...

Skill required: Life Sciences (AR&D) Services - SDTM Programming Designation: Associate Qualifications: Any Graduation,BE,BTech Years of Experience: 1-3 yrs About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do You will be aligned with our Life Sciences R&D vertical. Our services sp...

- UG/PG in Statistics, Mathematics, Life sciences, Engineering or Computer related subjects - Min. 6 yrs Exp in Statistical Programming-TLF,ADAM,SDTM,SAS Macros Developement CALL@WHATSAPP- RUKHSAR-9899875055 SHRUTI- 9911988551 SUHANI-9911988552

Role Summary/Purpose: AVP, Acquisition Credit Strategy will have the opportunity to work on major business initiatives in the Credit Acquisition team that contribute to Synchrony Financials growth and productivity objectives. You will be responsible for developing, delivering , validating & monitor the performance of Acquisition strategies. This role enables you to work directly with the business in catering to the end-to-end analytical needs and will have the opportunity to work with cross-functional teams and leverage state of the art tools (viz., SAS, FICO AWB) and expected to manage communication rhythm with stakeholders on a regular basis. This is an Individual Contributor role and repo...

Description. Principal Stat Programmer. Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers,...

Keysight Technologies is looking for R&D Engineer 1, Software to join our dynamic team and embark on a rewarding career journey Analyzing customer needs to determine appropriate solutions for complex technical issues Creating technical diagrams, flowcharts, formulas, and other written documentation to support projects Providing guidance to junior engineers on projects within their areas of expertise Conducting research on new technologies and products in order to recommend improvements to current processes Developing designs for new products or systems based on customer specifications Researching existing technologies to determine how they could be applied in new ways to solve problems Revie...

Keysight Technologies is looking for R&D Engineer 1, Software to join our dynamic team and embark on a rewarding career journey Analyzing customer needs to determine appropriate solutions for complex technical issues Creating technical diagrams, flowcharts, formulas, and other written documentation to support projects Providing guidance to junior engineers on projects within their areas of expertise Conducting research on new technologies and products in order to recommend improvements to current processes Developing designs for new products or systems based on customer specifications Researching existing technologies to determine how they could be applied in new ways to solve problems Revie...

As a Senior Principal Statistical Programmer, you will have the opportunity to work with advanced technical solutions such as R, Shiny, and SAS, allowing you to lead asset teams and mentor junior staff effectively. In this role, you will contribute to global assets across a variety of therapeutic areas, shaping strategic decisions in statistical programming. Your responsibilities will include leading the trial or asset programming team as the Lead Statistical Programmer, ensuring that asset and trial delivery aligns with established timelines and quality standards. You will perform programming activities at both trial and asset levels, including the development of SDTM and ADaM datasets and ...

Role & responsibilities Programming: Proficiency in both SAS and R languages, including syntax, data manipulation techniques, and statistical modeling. Data Analysis: Experience with data extraction from various sources, cleaning, preprocessing, and statistical analysis using SAS and R. Statistical Modeling: Ability to apply various statistical models, including linear regression and mixed-effects models, in both SAS and R. Reporting and Visualization: Experience with creating reports (e.g., using Qlik or R Markdown) and visualizations to communicate findings effectively Troubleshooting: Strong analytical and problem-solving skills to troubleshoot and resolve complex issues in SAS and R code...

Location : Vijayawada , Andhra Pradesh Office timings : 1:30 Pm to 10 PM Client details : Channelsoft IT services Pvt Ltd Domain: Health Care (Clinical Trails) About Channelsoft Channel Soft is a pioneer in IT outsourcing and offshore software development business that envisioned and instigated the adoption of the flexible business practices that today enable our client companies to operate more efficiently and produce more value. Currently in India we have employees around 550+ working on various technologies like java,.net , DB, BI, AWS and support team . Office address : Nagarjuna nagar , near NTR university , Vijayawada . Responsibilities For Clinical SAS Programmer: Creating and executi...

Job Summary We are seeking a skilled SAS Developer to join our team. The ideal candidate will have extensive experience in Base SAS, SAS Data Integration (DI), Extract, Transform, Load (ETL) processes, SAS Visual Analytics (VA), SAS Administration, and SQL. This role involves developing, implementing, and maintaining data integration solutions, performing ETL processes, creating insightful visual analytics, managing the SAS environment, and ensuring seamless data operations. Key Responsibilities Develop and maintain programs using Base SAS for data manipulation, analysis, and reporting. Optimize SAS code for performance and efficiency. Debug and troubleshoot SAS programs to resolve issues. D...

Role Summary Measuring, analyzing, and summarizing risk results for the bank's central credit risk reports - that's our job in CRM Quantification in Enterprise Risk Management Role Description As a Risk Portfolio Senior Specialist you will support the development of our analytics capabilities as well as monitor the development of credit portfolios and their risk parameters. Our team prepares analyses and reports to evaluate portfolio quality and risk concentration and to ensure that the credit risk strategy implementation complies with regulatory requirements and internal guidelines. You will be responsible for production and maintenance of regular / adhoc portfolio reports. Additionally sup...

Biostatistician cum Statistical Programmer Job Description Performs biostatistical and SAS programming activities for given clinical trials involving Novel, Biosimilar and PMS studies. As a Biostatistician cum Statistical Programmer youll work on a variety of projects, while collaborating with our cross-functional team of experts. You’ll be able to develop your statistical skills, gain exposure to multiple therapeutic areas. You’ll also contribute to research design and analytical strategies, provide input into protocols, Statistical Methodology and develop and review statistical analysis plans. As a Statistical Programmer, you will leverage your SAS programming skills to support Phase I-IV ...

The Associate Statistical Programmer will work with Medical Affairs biostatisticians and/or programmers and Sanofi Business Operations biostatistics and programming personnel to implement statistical analysis plans and provide QC d data packages including tables, figures, and listings for use in publications (ie abstracts, posters, oral, presentations, manuscripts, and ad-hoc data analysis requests) ; The Associate Statistical Programmer will assist in developing, implementing of programming techniques. The Associate Statistical Programmer will ensure SOPs are followe'd and that timelines and quality standards are met. People: 1) Develop and maintain effective relationships and collaboration...

Select how often (in days) to receive an alert: Select how often (in days) to receive an alert: Who we are The opportunity The Clinical Programming Lead Manager is responsible for managing timely and accurate execution of all start-up activities and milestone deliverables for all assigned clinical trial projects. Clinical Programming lead manager is responsible for data definition by working with CRO and Third-Party Vendors (TPV) to ensure receipt of data in Teva data standard format, generating the database transfer specification (DTS), receiving and processing study related data. This position is also responsible for providing professional expertise and leadership through leading departmen...

Salary : 2.2LPA - 14k Change in Hand per month (after deductions of PF,ESI,PT) 2Years Bond & Need to Submit your 10th Original Mark list with us during the Bond Period. Must have a SAS training Certificate. Role & responsibilities: 1. Providing inputs related to statistical methods for various study design ( two way, parallel, replicate, study state etc) and protocol preparation considering the requirements of BE studies for USFDA, EMEA, CANADA etc submission. 2. Preparation of randomization schedule as per the protocols and applicable SOPs for following study designs ( two way, parallel, replicate, study state etc). 3. Data checking for consistency and outlier analysis for bio-analytical da...

Clinical Data Programming Lead (SAS + EDC) - Bangalore/Chennai (Hybrid) The Clinical Data Programming Lead role is part of the Investigator Payments Group (IPG) and will be involved in the programming, delivery and oversight of data integration solutions between the Electronic Data Capture (EDC) system, the Clinical Trial Management System (CTMS) and our payment entitlement calculation system (APECS). The Clinical Data Programming Lead provides support to and acts as a back-up for the IPG Manager. To effectively assist the IPG Manager in leading the activities for those under his/her jurisdiction in a manner that ensures all timeframes and targets are met. The Clinical Data Programming Lead ...

Clinical Data Programming Lead (SAS + EDC) - Bangalore/Chennai (Hybrid) 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 The Clinical Data Programming Lead role is part of the Investigator Payments Group (IPG) and will be involved in the programming, delivery and oversight of data integration solutions between the Electronic Data Capture (EDC) system, the Clinical Trial Management System (CTMS) and our payment entitlement calculation system (APECS). The Clinical Data Programming Lead p...