407 Base Sas Jobs - Page 2

Develop and maintain complex statistical models and data visualizations using SAS.Collaborate with cross-functional teams to design and implement data-driven solutions.Analyze large datasets to identify trends and patterns,. Required Candidate profile Strong proficiency in SAS programming language,including Base SAS, Enterprise Guide, and Macros.Strong communication and collaboration,with the ability to work effectively with cross-functional teams.

Design, develop, and maintain complex statistical analysis systems using SAS.Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Required Candidate profile Strong knowledge of SAS programming language and its applications in clinical trial data management. Experience with SQL database management systems and querying languages.

Design, develop, and maintain complex statistical analysis systems using SAS.Collaborate with cross-functional teams to ensure timely delivery of high-quality results.Develop and implement efficient data processing Required Candidate profile Strong knowledge of SAS programming language and its applications in clinical trial data management. Experience with SQL programming language and database management systems.

Develop and maintain SAS programs for clinical trial data management, including data cleaning, transformation, and visualization.Collaborate with cross-functional teams to ensure timely delivery of high-quality deliverables. Required Candidate profile Strong knowledge of SAS programming language, including Base SAS, Enterprise Guide, and Macros. Experience with clinical trial data management systems, such as CDISC or Oracle Argus Safety.

Design, develop, and implement clinical trial data management systems using CDMS expertise.Collaborate with cross-functional teams to ensure seamless integration of clinical data management systems. Required Candidate profile Strong understanding of clinical trial data management principles and practices. Proficiency in CDMS, SAS programming language, and SQL database management systems.

Develop and maintain databases, spreadsheets, and reports for tracking and analyzing clinical trial data.Collaborate with cross-functional teams to ensure accurate and timely delivery of high-quality results. Required Candidate profile Strong knowledge of SAS programming language and its applications in clinical trial data analysis. Experience with Veeva or similar systems is desirable.

Analyze and interpret complex clinical trial data to inform business decisions.Develop and maintain databases, spreadsheets, and reports using SAS and Veeva.Collaborate with cross-functional teams Required Candidate profile Strong proficiency in SAS programming language and Veeva software. Experience working with large datasets and performing complex data analysis tasks. Excellent problem-solving skills

Design, develop, and implement clinical trial data management systems using SAS.Develop and maintain databases for clinical trial data, ensuring data quality and integrity.Collaborate with cross-functional teams Required Candidate profile Strong knowledge of SAS programming language, including Base SAS and Enterprise Guide. Experience with clinical trial data management, statistical analysis, and database development.

Design, develop, and implement clinical data programming solutions using R/SQL.Collaborate with cross-functional teams to ensure accurate and timely delivery of projects.Develop and maintain complex databases and data systems. Required Candidate profile Strong knowledge of R/SQL and its applications in clinical data programming. Experience working with large datasets and developing scalable solutions. Excellent problem-solving skills

Design, develop, and maintain clinical data systems using R/SQL.Collaborate with cross-functional teams to ensure data quality and integrity.Develop and implement data validation and verification processes. Required Candidate profile Strong knowledge of R/SQL programming languages. Experience working with clinical data systems and databases. Understanding of data modeling and data warehousing concepts.

Design, develop, and maintain complex statistical analysis systems using SAS.Collaborate with cross-functional teams to ensure timely delivery of high-quality results.Develop and implement data validation and quality control processes Required Candidate profile Strong knowledge of SAS programming language and its applications in clinical trial data management. Experience with SQL database management systems and data analysis tools.

Design, develop, and implement data models and algorithms to solve complex problems. Write efficient and well-documented code in R and SAS. Collaborate with cross-functional teams to identify business requirements Required Candidate profile Strong knowledge of R and SAS programming languages. Experience with data structures, algorithms, and software design patterns. Excellent problem-solving skills and attention to detail.

Analyze and interpret complex clinical trial data to inform business decisions.Develop and maintain databases, spreadsheets, and reports using SAS and Veeva.Collaborate with cross-functional teams to design Required Candidate profile Strong knowledge of SAS programming language and Veeva software. Experience working with large datasets and performing complex data analysis tasks. Excellent problem-solving skills

Design, develop, and implement data models and algorithms to solve complex problems.Collaborate with cross-functional teams to identify business requirements and develop solutions.Develop and maintain large-scale data systems Required Candidate profile Strong proficiency in R and SAS programming languages. Experience with data structures, algorithms, and software design patterns. Excellent problem-solving skills and attention to detail.

Develop and maintain SAS programs for clinical trial data management, including data cleaning, transformation, and visualization. Collaborate with cross-functional teams to ensure timely delivery of high-quality deliverables. Required Candidate profile Strong knowledge of SAS programming language, including Base SAS, Enterprise Guide, and Macros. Experience with clinical trial data management systems, such as CDISC or Oracle Argus Safety.

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. Excellent analytical, problem-solving, and communication skills. Ability to work independently and as part of a team.

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. 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.

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 maintain SAS programs for clinical trial data management and analysis. Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Required Candidate profile Experience working with clinical trial databases and data management systems. Excellent problem-solving skills and attention to detail.

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 Develop and maintain complex statistical analysis plans and reports using SQL. Troubleshoot and resolve technical issues related to clinical trial data management.

Analyze and interpret complex clinical trial data to inform business decisions.Develop and maintain databases, spreadsheets, and reports using SAS and Veeva.Collaborate with cross-functional teams Required Candidate profile Strong understanding of clinical trial design, protocols, and statistical analysis plans. Proficiency in programming languages such as SAS and Veeva. Experience with data management systems

Design, develop, and implement clinical trial data management systems using SAS.Collaborate with cross-functional teams to ensure accurate and timely delivery of project resultsDevelop and maintain complex databases using SQL Required Candidate profile Strong knowledge of clinical trial data management, statistical analysis, and database development. Proficiency in SAS programming language and SQL. Experience working with large datasets

Design, develop, and implement Veeva EDC clinical programming solutions for clients.Collaborate with cross-functional teams to ensure seamless integration of EDC systems.Develop and maintain technical documentation Required Candidate profile Strong knowledge of Veeva EDC clinical programming principles and practices. Experience with EDC system implementation and maintenance. Excellent problem-solving skills and attention to detail.

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

Design, develop, and implement clinical trial data management systems using CDMS expertise. Collaborate with cross-functional teams to ensure seamless integration of clinical data into the overall study design. Required Candidate profile Strong understanding of clinical trial data management principles and regulations. Proficiency in CDMS and SAS programming languages with at least 2 years of experience.