707 Sas Programming Jobs - Page 7

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

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 Required Candidate profile Strong proficiency in R and SAS programming languages. Experience working with large datasets and complex data systems. Excellent analytical, problem-solving, and communication skills.

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.

Develop and maintain complex data models using R and SAS programming languages. Analyze large datasets to identify trends and patterns, providing insights to stakeholders. Design and implement data visualizations to effectively communicate results. Required Candidate profile Strong proficiency in R and SAS programming languages. Experience working with clinical trial data and regulatory requirements.Excellent analytical and problem-solving skills with attention to detail.

Develop and maintain complex data analysis systems using R and SAS programming languages. Collaborate with cross-functional teams to design and implement data-driven solutions. Required Candidate profile Strong proficiency in R and SAS programming languages. Experience working with large datasets and complex data analysis systems.

Develop and maintain complex data analysis systems using R and SAS programming languages. Collaborate with cross-functional teams to design and implement data-driven solutions. Required Candidate profile Strong proficiency in R and SAS programming languages. Experience working with clinical trial data and regulatory requirements. Excellent analytical, problem-solving, and communication skills.

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 data models and algorithms to solve complex problems. Collaborate with cross-functional teams to identify business needs and develop solutions. Develop and maintain large-scale databases and data systems. Required Candidate profile Strong proficiency in R and SAS programming languages. Experience with data analysis and interpretation. Excellent problem-solving skills and attention to detail.

Develop and maintain complex statistical models and algorithms using R and SAS. Design and implement data visualizations to effectively communicate insights to stakeholders. Collaborate with cross-functional teams . Required Candidate profile Strong proficiency in R and SAS programming languages. Experience with data visualization tools such as Tableau or Power BI.

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.

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.

Develop and maintain complex data analysis systems using R and SAS programming languages. Collaborate with cross-functional teams to design and implement data-driven solutions. Analyze large datasets to identify trends, patterns. Required Candidate profile Strong proficiency in R and SAS programming languages with experience in clinical data analysis. Excellent problem-solving skills and attention to detail are required to analyze complex data sets.

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.