407 Base Sas Jobs - Page 3

Design, develop, and implement clinical SAS programs for data management and analysis. Develop and maintain complex SQL databases for data storage and retrieval. Required Candidate profile Strong expertise in CDMS, clinical SAS programming, and SQL database management. Experience working with large datasets and developing complex data models.

Design, develop, and implement data programming solutions using SAS. Collaborate with cross-functional teams to identify business requirements and develop effective data programming strategies. Required Candidate profile Strong proficiency in SAS programming language, including data manipulation, transformation, and visualization. Experience working with large datasets, focusing on data quality and integrity.

Design, develop,and implement statistical models and data visualizations using SAS. Collaborate with cross-functional teams to identify business needs and develop solutions. Develop and maintain complex programs using R and SAS. Required Candidate profile Strong proficiency in SAS programming language. Experience with R programming language is desirable. Excellent analytical and problem-solving skills.

Analyze and interpret complex clinical trial data using SAS. Develop and maintain databases, data systems, and computer models for clinical trial management. Collaborate with cross-functional teams. Required Candidate profile Strong proficiency in SAS programming language. Experience with Veeva or similar clinical trial management systems. Excellent analytical, problem-solving, and communication skills.

Develop and implement statistical analysis plans for clinical trials. Conduct statistical programming activities, including data management, reporting, and visualization. Required Candidate profile Strong knowledge of biostatistics and statistical programming principles. Experience working with large datasets and complex statistical models.

Design, develop, and implement clinical trial data management systems using SAS. Collaborate with cross-functional teams to ensure seamless integration of clinical data into the development process. Required Candidate profile Strong proficiency in SAS programming language and its applications in clinical trial data management. Experience with SQL programming language and its applications in statistical analysis.

Design, develop, and implement Veeva EDC clinical programming solutions for clients. Collaborate with cross-functional teams to ensure seamless integration of Veeva EDC ystems. Required Candidate profile Strong understanding of Veeva EDC principles and technologies. Experience with clinical trial data management systems. Excellent problem-solving skills and attention to detail.

Develop and implement statistical analysis plans for clinical trials. Conduct data review and quality control checks to ensure accuracy and completeness. Collaborate with cross-functional teams to design and execute studies. Required Candidate profile Strong knowledge of statistical concepts and methodologies. Experience working with clinical trial data and statistical software. Excellent communication and interpersonal skills.

Analyze complex data sets using R and SAS tools to identify trends and patterns. Develop and implement data models and algorithms to solve business problems. Collaborate with cross-functional teams to design and implement data-driven solutions. Required Candidate profile Strong proficiency in R and SAS programming languages. Experience with data modeling, data visualization, and statistical analysis. Excellent problem-solving skills and attention to detail.

Analyze complex data sets using R and SAS tools to identify trends and patterns. Develop and maintain databases, data systems, and computer models to support business operations. Collaborate with cross-functional teams to design Required Candidate profile Strong proficiency in R and SAS programming languages. Experience with large datasets and complex data analysis techniques. Excellent problem-solving skills and attention to detail.

Develop and implement statistical analysis plans for clinical trials. Conduct statistical reviews of case report forms, annotated CRFs, database structures, and study-related documentation. Collaborate with cross-functional teams Required Candidate profile Strong knowledge of statistical concepts, techniques, and tools. Experience in the employment firm or recruitment services industry is preferred. Excellent communication and interpersonal skills

Develop and implement statistical analysis plans for clinical trials. Conduct statistical reviews of case report forms, annotated CRFs, database structures, and study-related documentation. Collaborate with cross-functional teams Required Candidate profile Strong understanding of biostatistics principles and methodologies. Experience working with clinical trial data and statistical software packages. Excellent communication and interpersonal skills.

Analyze complex data sets using R and SAS tools to identify trends and patterns. Develop and maintain databases, data systems, and reports to support business decisions. Collaborate with cross-functional teams to design Required Candidate profile Strong proficiency in R and SAS programming languages. Experience with data visualization tools such as Tableau or Power BI. Excellent analytical, problem-solving, and communication skills.

Design, develop, and maintain SAS programs for clinical trial data management and analysis. Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Develop and implement data validation and quality control Required Candidate profile Strong knowledge of SAS programming language and its applications in clinical trial data management and analysis. Experience working with clinical trial databases and data management systems.

Design, develop, and implement clinical trial data management systems using CDMS expertise. Collaborate with cross-functional teams to ensure seamless integration of clinical trial data into the overall study design. Required Candidate profile Strong understanding of clinical trial data management principles and CDMS expertise. Proficiency in SAS programming language with experience in developing complex statistical analysis plans.

Develop and implement statistical analysis plans for clinical trials. Conduct statistical programming activities, including data management, reporting, and visualization. Collaborate with cross-functional teams to ensure timely Required Candidate profile Strong knowledge of biostatistics and statistical programming principles. Excellent analytical, problem-solving, and communication skills. Ability to work independently and as part of a team.

Design, develop, and implement clinical SAS programs for data management and analysis. Develop and maintain complex SQL databases for data storage and retrieval. Collaborate with cross-functional teams to identify business requirements Required Candidate profile Strong proficiency in SAS programming language, including Base SAS, Enterprise Guide, and Macros. Experience with SQL database management systems, including design, development, and maintenance.

Design, develop, and maintain SAS programs for clinical trial data management and analysis. Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Develop and implement data validation Required Candidate profile Strong knowledge of SAS programming language and its application in clinical trial data management and analysis. Experience working with clinical trial databases and data management systems.

Contract Duration : 3 months Skills : - Snowflake, Teradata - Data Visualization like Tableau - SAS/Base, SAS Enterprise, SAS/Macros and SAS/SQL (OR) Python, SQL Responsibilities : - Interpret data, analyze results using statistical techniques, and provide ongoing reports. - Develop and implement databases, data collection systems, data analytics, and other strategies that optimize statistical efficiency and quality. - Acquire data from primary or secondary data sources and maintain databases/data systems. - Identify, analyze, and interpret trends or patterns in complex data sets. - Filter and "clean" data by reviewing computer reports, printouts, and performance indicators to locate and cor...

12 to 16 years of experience in Artificial Intelligence, Machine learning technologies, GenAI technologies. Proven experience as an Enterprise Architect, Solution Architect, or a similar role, with a focus on AI/ML and generative AI. Core expertise in architecting AI/ML, Deep learning & GEN AI Solutions end-to-end. Proven skills building machine learning, deep learning models leveraging large datasets. Extensive math and computer skills, with a deep understanding of probability, statistics, and algorithms. Proficiency in NLP and computer vision techniques to extract insights from unstructured clinical/healthcare data. Experience in designing algorithms for predictive analytics for efficient ...

Minimum 3-11 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

Design develop data visualizations using Alteryx Tableau Collaborate with stakeholders to understand data needs translate them into actionable insights Clean, prepare, analyze large datasets using Alteryx Create interactive dashboards reports that effectively communicate insights

Hi , We are hiring for Leading ITES Company for SDTM Programmer Profile. To Apply, WhatsApp 'Hi' @ 9151555419 Follow the Steps Below: >Click on Start option to Apply and fill the details >Select the location as Other ( to get multiple location option ) a) To Apply for above Job Role ( Mumbai ) Type : Job Code # 208 b) To Apply for above Job Role ( Pune ) Type : Job Code # 209 Key Skills : Looking for an SDTM programmer with Min 3 + years experience in SDTM programming and SAS programming Should have good knowledge of CDISC standards, Trial Design domains, Define Qualifications - Health Care Professional OR Masters/Bachelor’s degree in Life Sciences/Physician Please go through the JD and we w...

Main responsibilities: The Senior 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 QCd data packages including tables, figures, and listings for use in publications (i.e. abstracts, posters, oral, presentations, manuscripts and ad-hoc data analysis requests); The Senior Statistical Programmer will develop, implement, and document non-routine macros and advanced techniques; The Senior Statistical Programmer will ensure SOPs are followed and timelines and quality are met. People: 1) Develop and maintain effective relationships and c...

About The Role Project Role Application Developer Project Role Description Design, build and configure applications to meet business process and application requirements. Must have skills SAS Base & Macros Good to have skills NA Minimum 3 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. A typical day involves collaborating with team members to understand project needs, developing application features, and ensuring that the applications function smoothly and efficiently. You will also engage in problem-solving di...