474 Sas Programming Jobs - Page 15

locationsHyderabad, India posted onPosted Yesterday job requisition idR-446112 About this role: Wells Fargo is seeking a Lead Analytics Consultant People Analytics. As a consultant, you will work as analytics professional in HR People Analytics and Business Insights delivery team and will be responsible for effective delivery of projects as per the business priority. The incumbent is expected to be an expert into executive summary, people strategy, HR consulting, HR advisory, advanced analytics & data science and value addition to the projects. In this role, you will: Advise line of business and companywide functions on business strategies based on research of performance metrics, trends in ...

Job Description : As a biotechnology trailblazer, we're dedicated to discovering, developing, and commercializing cutting-edge gene and cell therapies, and biologics to transform global healthcare. If you're ready to be part of a team that's shaping the future of medicine and making a profound impact on patient lives worldwide, join Ocugen and well rewrite the future of healthcare together. Job purpose : The Statistical Programmer will be responsible for providing statistical services including analysis, interpretation, design, and reporting or communication of data evidence for research, development, and/or marketed product. The individual should be able to ensure application of appropriate...

ROLES and RESPONSIBILITIES: Perform review of Protocol, Case Report Forms, annotated Case Report Forms, Statistical Analysis Plan, and mock shell Develop and/or validate SDTM domains and ADaM datasets as per the specifications for both Safety and efficacy •Develop and/or validate Tables, Listings, and Figures using SAP and mock shells •Create or review P21 reports, define packages [Define.xml] and Reviewers guide [RGs] for CDISC Data Standards •Ability to work independently and as part of a team environment •Provide the status of assigned tasks to the Study Lead Programmer •Actively participating in the study meetings and support as backup lead •Identify, communicate, and manage study-based ...

We are hiring for TOP MNC for Clinical Sas programmer / Clinical Data. Work Location- Bangalore. Years of experience- 4- 10 Years Education qualification: Life Science Graduates ( Bpharm, Mpharm, Pharm D, Bsc ( Biotechnology), BE (Biotechnology). Domain : Life Science Salary Range: 4- 6 Years - 5LPA - 9LPA. 6- 10 Years- 8LPA- 13LPA 7- 11 Years- 12- 18LPA Notice Period- Immediate - 30 Days. Work Mode- Work from office. Shift- Should be flexible including night. Skills Required . Must have relevant experience in Clinical SAS. Should have experience in Macros & ProcSQL. Must have knowledge of clinical trials. Good communication skills. Interested candidates please share resume on below details....

Title Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based SAS Programmer to join our Biostatistics team in India, Mumbai. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of...

Title Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Statistical Programming Manager to join our Biostatistics team in India, Mumbai. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the glob...

Title Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Senior SAS Programmers to join our Biostatistics team in India, Mumbai. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global develo...

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. Location: Home-based 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 Biostatis...

Job Location: Ahmedabad Job Role for Biostatistician: 1. Provide inputs regarding sample size, study design, randomization and PK-statistical analysis in protocol. 2. Prepare randomization schedule using SAS for the project as per the protocol. 3. Perform and review statistical analysis of pharmacokinetic pharmacodynamic parameters using phoenix WinNonlin or SAS. 4. Prepare summary and final reports for the study. 5. Perform the validation of the SAS codes and softwares used for calculation and analysis of Pharmacokinetic and statistical data. 6. Maintain all necessary records for the reporting phase of the study. 7. Prepare inputs in sample analysis detail Preferred Candidate: M.Sc(Statisti...

Role & responsibilities Designing and implementing clinical data collection systems and tools Coordinating with investigators and other healthcare professionals to gather and interpret clinical data Overseeing the data management process, including data collection, entry, verification, and cleaning Ensuring the integrity, accuracy, and security of all clinical data Preparing and maintaining documentation related to data management activities, such as data management plans and standard operating procedures Ensuring compliance with regulatory standards and guidelines, including Good Clinical Practice (GCP) Working closely with biostatisticians and other data scientists to analyze clinical data...

What you'll be doing Create, test and maintain SAS codes used to create and/or validate statistical outputs for the cardiac safety statistical analysis; create and maintain procedures for creation of TFLs/ statistical outputs; provide statistical support under the supervision of senior team resources and/or department management; may supervise staff in a line management or matrix capacity. Develop, test, execute and maintain SAS and R programs for statistical analysis including central tendency analysis, categorical analysis, and concentration-QTc analysis Validate results of statistical analysis by double programming Prepare tables, figures, and listings for statistical analysis as outlined...

As a Principal Statistical Programmer, you'll be at the forefront of developing and validating programs that create datasets conforming to Alexion and ADaM specifications. Your expertise will drive the analysis of efficacy data through Tables, Listings, and Figures (TLFs). you'll ensure compliance with ICH guidelines, Good Clinical Practices, and regulatory requirements while leading programming efforts and representing Clinical and Statistical Programming in meetings with internal and external clients. As a mentor to other Statistical Programmers, you'll integrate statistical concepts with SAS Programming efficiently and optimally. Accountabilities: Develop and validate technical programmin...

About the job The role is based in the Pune R&D Center, at SAS R&D Pune facility, SAS9 team. We are looking for an SDET to validate SAS9 ARD software, install/migration process on Windows and Unix platforms along with automating the functional test sets for the SAS 9 platform based (ARD) solutions. You will be joining a friendly team with a broad range of experience, to develop and maintain SAS 9 Solutions. Required Qualifications A minimum of 2-4 years of experience in all facets of software testing in a product-based software development environment SAS Technologies: Base and Advance SAS and SAS Macro Programming Knowledge of performance tuning techniques on SAS Understanding of testing co...

Statistics & Data Corporation (SDC), a specialized contract research organization (CRO) headquartered in Arizona, delivering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005. SDC providing a technology enabled service offering to provide clients with both clinical services expertise, as well as the technology they need to be successful in their clinical trials. Job Summary Provide statistical programming support to clinical trials. Produce statistical analyses, including generating/validating analysis datasets, tables, listings, and figures for clinical trials. Create SDTM mapping and datasets. Develop and maintain the infrastru...

Job Title: Senior Statistical Programmer II Career Level: D Introduction to role: Are you ready to make a significant impact in the world of rare disease biopharma? As a Senior Statistical Programmer II, youll be at the forefront of developing and validating programs that create datasets conforming to Alexion and CDISC standards. You will play a pivotal role in generating Tables, Listings, and Figures for analysis purposes. Depending on the complexity of the study, you may lead programming projects, ensuring adherence to ICH guidelines, Good Clinical Practices, and regulatory requirements. Your expertise will guide and mentor junior programmers, while your ability to integrate statistical co...

: Job TitleTest Analyst Corporate TitleAVP LocationPune, India Role Description EngineerTechnical specialist What we'll offer you As part of our flexible scheme, here are just some of the benefits that youll enjoy, Best in class leave policy. Gender neutral parental leaves 100% reimbursement under childcare assistance benefit (gender neutral) Sponsorship for Industry relevant certifications and education Employee Assistance Program for you and your family members Comprehensive Hospitalization Insurance for you and your dependents Accident and Term life Insurance Complementary Health screening for 35 yrs. and above Your key responsibilities Liaising with technical architects to develop strong...

Job Summary: Were looking for a SAS Data Integration (DI) Developer to join our team. In this role, you'll be responsible for designing and optimizing ETL processes using SAS DI Studio, as well as automating job schedules. Youll work with large datasets, ensure data integrity, and collaborate with cross-functional teams to meet business requirements. Additionally, you'll troubleshoot and monitor jobs while ensuring adherence to data governance standards. If you're excited to work in a dynamic and growing environment, this is a great opportunity to apply your skills to cutting-edge technologies. Key Responsibilities: Develop and maintain ETL processes using SAS DI Studio. Design and optimize ...

Job Description: Role Title: AVP, Analytics - H&W Platform (L10) 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 also been recognized by Ambit...

Role : Name: Open Source Transition Lead Office : Client Deployed Mode : Hybrid Location : Banglore. Note: This role is an opportunity to Client Deployed model under EY payrolls. This is a initial duration of 6 months role, the tenure is subject to extension basis performance. Job Responsibility: • Transition from Sas to open source • Adopting R as open-source language Python • Scope is R&D wide ( 1000+ users) • Upskilling, right tools and program themselves and standard tools • Systems have Sas code and need to be decommissioned Big tech component • Business and Tech change • User engagement, comms, and training and getting voice of Customer (making training program. Please share ur updated...

XpertDox is a big-data healthcare start-up based out of Birmingham, AL, USA. We use advanced data analytics and proprietary natural language processing to structure, parse and map information from multiple diverse data sources. Its proprietary search engine and mappings are used to improve access to clinical trials and automate the coding process. We are seeking a SAS Programmer to become an integral part of our team! Responsibilities: SAS programming and debugging Creating automated SAS scripts and batch runs Perform QC on SAS batch exports Document all programming tasks and procedures Qualifications: Previous experience in SAS programming Familiarity with relational and non-relational data...

Role & responsibilities Developing, testing, validating, and maintaining SAS programs to generate analysis datasets, tables, listings, and figures Working closely with data management and statistical teams to understand the requirements for each project Reviewing clinical trial data and addressing any data inconsistencies or errors Designing and implementing strategies to manage, clean and verify clinical trial data Performing statistical analysis on clinical trial data Creating and maintaining documentation for all SAS programs and processes Ensuring that all programming activities and processes performed are conducted according to standard operating procedures and good programming practice...

Job Title: Senior Statistical Programmer II Career Level: D Introduction to role: Are you ready to take on a pivotal role in the development and validation of programs that create datasets conforming to Alexion and CDISC standards? As a Senior Statistical Programmer II, you will be at the forefront of crafting Tables, Listings, and Figures (TLFs) for analysis purposes. Depending on the projects size and complexity, you may lead programming efforts, ensuring alignment with ICH guidelines, Good Clinical Practices, and regulatory requirements. Youll also have the opportunity to mentor fellow programmers and represent Statistical Programming in meetings with internal and external clients. Are yo...

This position is for a Manager with an advanced degree in a quantitative discipline; requires experience and proficiency in areas of statistics, applied mathematics, SAS programming language and a good understanding of retail banking / small business lending businesses. The individual will use these skills in the development of risk models (IRB, IFRS9, Custom Scorecards and others) and other risk analytics in retail banking / small business lending portfolios. Responsibilities include developing statistically derived predictive models, perform decision tree-based customer segmentation & profiling analyses, assist business implementation of sophisticated Regulatory and Scoring models and prov...

Job Title: Senior SAS Programmer Experience: 510 Years Location: Bangalore (BLR) Notice Period: 0–30 Days Employment Type: Full-time Job Summary: We are looking for a Senior SAS Programmer with strong experience in clinical trial data programming. The ideal candidate will have expertise in SAS, SQL, and statistical reporting to support data analysis for clinical research studies. You will work closely with biostatisticians, data managers, and clinical teams to ensure the accuracy and quality of clinical trial outputs. Key Responsibilities: Develop and validate SAS programs to generate statistical summary tables, listings, and graphs (TLGs) . Create derived datasets for analysis using complex...

Important Points to be noted here before you apply for this job:- 1. This is a 3rd Party Pay-roll opportunity, wherein, the Consultant will be on pay-rolls of Zentek Infosoft and working for the end client of Infosys. Apply ONLY if you are fine to work as a Sub Contractor on 3rd Party Pay-roll . 2. This is a LONG-TERM Opportunity with a Strong Chance of getting converted as Full Time Opportunity with Infosys after few months . 3. One round of Face-to-face Interview is a MUST for this role. 4. This is a Work from Office opportunity and person is expected to work from one of these offices of Infosys - Bangalore. This is NOT a Hybrid or WFH opportunity . We have Offshore Credit Risk requirement...