190 Proc Sql Jobs - Page 3

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.

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.

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.

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.

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.

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.

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

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

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

You have a job opportunity where you will be expected to have a minimum of 3-5 years of work experience in SAS EG and SAS CI. Your responsibilities will include hands-on experience in transferring data from various sources to a SAS database. It is essential for you to have expertise in Data Step and Proc Step, including merge statement proc sql, macros, and SAS functions. In addition, you should have experience in automation and SAS reporting. Good communication skills are a must as you will be required to work independently to deliver project work and interact with clients. The location for this position is any Infosys DC in India. Key Responsibilities: - Minimum 3-5 years of work experienc...