474 Sas Programming Jobs - Page 5

Roles and Responsibility Design, develop, and implement statistical models using R and SAS. Collaborate with cross-functional teams to identify business problems and provide solutions. Develop and maintain large-scale data systems and databases. Write efficient and well-documented code. Troubleshoot and resolve technical issues. Participate in code reviews and contribute to improving overall code quality. Job Requirements Strong knowledge of R and SAS programming languages. Experience working with large datasets and databases. Excellent problem-solving skills and attention to detail. Ability to work collaboratively in a team environment. Strong communication and interpersonal skills. Familia...

About The Role Project Role : Application Designer Project Role Description : Assist in defining requirements and designing applications to meet business process and application requirements. Must have skills : SAS Analytics Good to have skills : NAMinimum 3 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Designer, you will assist in defining requirements and designing applications to meet business process and application requirements. Your typical day will involve collaborating with various stakeholders to gather and analyze requirements, creating design specifications, and ensuring that the applications align with busine...

Main responsibilities: The Principal Biostatistician will work with Medical Affairs biostatisticians and/or programmers and Sanofi Business Operations biostatistics and programming personnel to implement statistical analysis plans (SAP), programming specifications for analysis datasets and provide QC done data packages including tables, figures, and listings for use in publications (i.e., abstracts, posters, oral, presentations, manuscripts and ad-hoc data analysis requests) and to investigate the natural history of a TA diseases and long-term treatment outcomes of observational data using clinical trials and / or Registries as applicable; The Principal Biostatistician will ensure SOPs are f...

Main responsibilities: The Senior Biostatistician will work with Medical Affairs biostatisticians and/or programmers and Sanofi Global Hub biostatistics and programming personnel to implement (Develop and/or QC) statistical analysis plans(SAP), programming specifications for analysis datasets and provide QCd data packages including tables, figures, and listings for use in publications (i.e. abstracts, posters, oral, presentations, and manuscripts and ad-hoc data analysis requests) and to investigate the natural history of a TA diseases and long-term treatment outcomes of observational data using clinical trials and / or Registries as applicable) .The Senior Biostatistician will ensure SOPs a...

Grade: L2-2 About the job As Principal Data Standards Analyst within our Clinical Information Governance, As a member of a CIG (Clinical Information Governance) team, the Principal Data Standards Analyst acts as a metadata expert as he/she provides in-depth knowledge and guidance on clinical data standards (CDISC) and best practices for metadata management across global and study-specific levels. Understand the CDISC models (CDASH, SDTM, External Data, Controlled Terminology) and all regulatory requirements regarding Data Standards. Actively leads Therapeutic Area Working Groups. The Principal Data Standards Analyst will bridge the gaps between global metadata strategy and its adoption withi...

Role Overview: You are a boutique data analytics consultancy specialized in Health Economics and Outcomes Research (HEOR), pricing, and market access. Your clientele includes pharmaceutical and medical device companies, as well as midsize and large consultancies worldwide. Your dedicated team of expert health economists and systematic reviewers ensures the delivery of high-quality work within specified timelines. Key Responsibilities: - Conduct statistical analysis necessary for submissions to HTA agencies like NICE and PBAC. - Develop proposals, project reports, and various deliverables for clients. - Design, analyze, and interpret data utilizing a diverse range of statistical approaches an...

Role Overview: As a Statistical Programmer at Statistics & Data Corporation (SDC), 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. Key Responsibilities: - Overseeing statistical programming activities for medium to l...

Educational Requirements Bachelor of Engineering Service Line Data & Analytics Unit Responsibilities Minimum 3-5 years of work experience in SAS EG and SAS CI Hands on experience in data transferring from different sources to SAS database Expertise in Data Step and Proc Step including merge statement , proc sql and macros , SAS functions Experience in automation and SAS reporting Good communication skill is must. Candidate should independently work deliver the project work as well as deal with client . Location : Any Infosys DC in India Preferred Skills: Technology->ETL & Data Quality->ETL & Data Quality - SAS->SAS - SAS Data Integration Studio

Are you ready to make a difference in the world of biopharmaceuticalsAs a Statistical Programmer II, youll play a crucial role in developing and validating programs that create datasets conforming to Alexion and CDISC standards. Youll be responsible for generating Tables, Listings, and Figures for analysis purposes, ensuring adherence to ICH guidelines, Good Clinical Practices, and regulatory requirements. This position offers the opportunity to work on moderate scope and medium complexity studies or drug projects, contributing to continuous improvement within cross-functional teams. Under the guidance of an experienced programmer, youll enhance your understanding of statistical concepts and...

ARAI, Pune is a premier Automotive Research Institute, with the Ministry of Heavy Industries, involved in R&D, Homologation, Testing & Certification, Calibration & Skill Development services to Automotive and Allied industries globally, We are looking for the following position for our Noise Vibration and Harshness Laboratory (NVH): Designation: Research Engineer (NVH Testing) (01 ARAI Contract) Location: Pune Work Experience: 1-3 Years Candidates should have completed full time Post-graduation (ME or MTech)/Degree (BE or BTech)/Diploma in Engineering (Mechanical / Automobile / Production) with good track record of academic career with relevant experience of 1-3 years and good communication ...

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...

As a Statistical Programmer in our clinical research team, you will have the crucial responsibility of programming, validating, and delivering statistical outputs for clinical trials. Your role will involve ensuring compliance with regulatory standards and industry best practices. Key Responsibilities: - Develop and maintain SAS programs for clinical trial data processing, analysis, and reporting - Map clinical trial data to CDISC standards (SDTM and ADaM) to ensure regulatory compliance - Create and maintain analysis datasets following CDISC implementation guidelines - Perform data validation and quality control checks to uphold data integrity - Generate and maintain CDISC documentation inc...

Responsibilities This position requires an individual to do the following: Solution Architect who can come up with the framework for new automation projects Provides technical contribution and support in the customer Automation requirement Gains commitment from customer and Keysight for the technical solutions Uses good judgment to determine and develop technical approaches and techniques for solutions to customer problems Interacts with senior internal and external personnel Quick in response with the solutions to the customer queries

About The Role : Job TitleCDO/CLO Modeling Analyst LocationBangalore, India Role Description OverviewBusiness Division Deutsche Banks Corporate Bank (CB) a market leader incash managemnet, trade finance & lending, securities services and Trust & Agency Services. Focusing on the treasurers and finance departments ofcprporate and commercial clients and financial institutionsacross the globe, our universal expertise and global network allows us to offer truly integrated and effective solutions. OverviewBusinessTrust and Agency Service (TAS) With offices in New York, California, London, Frankfurt, Milan, Lisbon, Dublin, Hong Kong, Singapore and Tokyo, the Trust and Agency Services team at Deutsc...

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:- Raipur, chhatisgarh 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

As a Statistical Programming Manager at Medpace, based in Mumbai, India, within the Biostatistics team, you will have a crucial role in supporting project teams on programming matters. Your responsibilities will include 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. Key Responsibilities: - Support project teams on programming matters - Manage programming staff - Ensure high-quality delivery - Provide leadership and training for the Programming group - Lead the development of Programming standards to maximize efficiencies Qualifications Requi...

As a SAS Programmer at our expanding corporate activities in Mumbai, India, you will collaborate with a team in the Biostatistics department to complete crucial tasks and projects necessary for the company's success. Your main responsibilities will include: - Writing SAS programs to generate analysis datasets, tables, listings, and figures - Programming, validating, and maintaining mapped databases using SAS - Developing edit checks for external data and facilitating communication with Data Management regarding database specifications and data transfers To qualify for this position, you should have: - A Bachelor's or Master's Degree in math, Statistics, health informatics, data science, comp...

Your Role We are seeking an experienced and collaborative Senior Statistician I to provide advanced statistical expertise and leadership in support of clinical research studies. This role involves working closely with Biostatisticians, Statistical Programmers, Clinical Data Managers, and sponsor teams to ensure the accuracy, reliability, and regulatory compliance of statistical deliverables. The Senior Statistician will also oversee quality control processes and contribute to the development of statistical analysis plans and datasets. In this role, you will: Provide statistical leadership and support for clinical trials, ensuring high-quality deliverables. Participate in cross-functional stu...

Role Overview: You are being offered the opportunity to join as an Associate Director, PKPD / Pharmacometrics / NONMEM / SAS Programmer in the Clinical Pharmacology and Quantitative Pharmacology Data Programming team. Your main responsibility will be to prepare, program, validate, and diagnose data to support Pharmacometrics and Clinical Pharmacology analyses. Your influence will be vital in shaping crucial decision-making processes throughout all stages of drug development and regulatory interactions. Key Responsibilities: - Expertly clean, manipulate, transform, and integrate data at both the study and compound level to ensure accurate analysis. - Utilize advanced data integration techniqu...

- 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...

**Greetings from You & I Consulting!** We've proudly helped candidates build careers at 64+ top MNCs across India, and were excited to bring you a new opportunity with a leading global company. If you have experience in Statistical Programming, this role is your next step forward! Senior Lead Statistical Programmer!!! We are hiring for: Senior Lead Statistical Programmer up to 22LPA ctc **To Apply Call on Puja- 8167854231 /Or Whatsapp on the same Number with your CV** Experience Level: 4 to 18 years Location-Mumbai , Kochi, Bangalore and PAN India Job Description : We are seeking an experienced and driven Senior Lead Statistical Programmer with 1015 years of experience in clinical trial prog...

What You'll Bring: - Minimum 5 years of hands-on experience in Advance SAS/R programming. - Must have experience of R programming, R Package development, good knowledge of SQL - Working knowledge of Python is a big plus! - Excellent written and verbal communication skills. - Familiarity with TIBCO Spotfire or similar visualization toolscreating calculated columns, markings, filters, and document properties. Why Join Us? - Work on impactful projects that make a difference. - Collaborate with a team of passionate data professionals. - Flexible work environment with opportunities to grow and innovate.

Project Role : Application Developer Project Role Description : Design, build and configure applications to meet business process and application requirements. Must have skills : SAS Analytics Good to have skills : NAMinimum 3 year(s) of experience is required Educational Qualification : 15 years full time education1. Must Have Skills - SAS 9.x, SAS Viya, Windows, Linux, AIX, MAINFRAMEWe are looking for Admin2.Roles and responsibilities:SAS Environment Management:1. Install, configure, and upgrade SAS software (SAS 9.x, SAS Viya, etc.) across different platforms (Windows, Linux, AIX, etc.).2. Set up and maintain SAS metadata server, SAS object spawners, and SAS compute servers.3. Perform reg...

Role Overview: As AVP, Remediation Analytics at Synchrony, you will have the opportunity to work on major remediation projects with special focus on Credit functions. Your responsibilities will include understanding business requirements, building complex logics to identify and remediate the impacted population, and managing various projects within the framework of remediation analytics. Key Responsibilities: - Develop Advanced SAS and/or SQL code, visual basic macros or other query tools for remediation. - Support remediation projects by partnering with FRCs and cross-functional teams, understanding business requirements, and developing analytics solutions to identify impacted population an...

As a SAS Programmer at Catalyst Clinical Research, you will play a crucial role in providing SAS programming support for Statistics and Data Management functions related to clinical trials and regulatory submissions. Your responsibilities will involve collaborating closely with Biostatisticians and Data Managers to develop SAS programs for validating tables, listings, and figures, as well as assisting with data cleaning and query generation. Additionally, you will serve as a contact for programming activities within the organization. Key Responsibilities: - Perform data manipulation techniques and advanced programming techniques such as arrays, transpositions, complex merges, SQL, SDTM, etc....