339 Sas Macros Jobs - Page 6

Roles and Responsibility Analyze and interpret complex clinical data to inform business decisions. Develop and maintain databases, spreadsheets, and reports using SAS and Veeva. Collaborate with cross-functional teams to design and implement data analysis solutions. Ensure data quality, integrity, and compliance with regulatory requirements. Provide technical support and training to junior team members on data analysis tools. Stay up-to-date with industry trends and emerging technologies in clinical data analysis. Job Requirements Strong proficiency in SAS programming language and Veeva software. Experience working with large datasets and performing complex data analysis tasks. Excellent pro...

Roles and Responsibility 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 for EDC systems and applications. Troubleshoot and resolve issues related to EDC system performance and data quality. Provide training and support to end-users on EDC systems and applications. Participate in project planning, execution, and delivery to meet client requirements. Job Requirements Strong understanding of IT Service & Consulting principles and practices. Experience working with Veeva EDC clinical programming tools and technologies. Excellent...

Roles and Responsibility Design, develop, and implement Veeva EDC clinical programming solutions for clients. Collaborate with cross-functional teams to identify and prioritize project requirements. Develop and maintain high-quality code that meets client specifications and industry standards. Troubleshoot and resolve technical issues related to Veeva EDC clinical programming. Provide training and support to clients on the use of Veeva EDC clinical programming tools. Participate in the development of best practices and standards for Veeva EDC clinical programming. Job Requirements Strong understanding of Veeva EDC clinical programming principles and methodologies. Experience working with var...

Roles and Responsibility Design, develop, and implement Veeva EDC clinical programming solutions for clients. Collaborate with cross-functional teams to identify and prioritize project requirements. Develop and maintain high-quality code that meets client specifications and industry standards. Troubleshoot and resolve technical issues related to Veeva EDC clinical programming. Provide training and support to clients on the use of Veeva EDC clinical programming tools. Stay up-to-date with industry trends and emerging technologies in Veeva EDC clinical programming. Job Requirements Strong knowledge of Veeva EDC clinical programming principles and practices. Experience working with IT Service &...

Roles and Responsibility Design, develop, and implement clinical trial data management systems using Veeva EDC. Collaborate with cross-functional teams to ensure seamless integration of clinical data into the development process. Develop and maintain high-quality, accurate, and timely clinical trial data. Troubleshoot and resolve issues related to clinical data management and reporting. Ensure compliance with regulatory requirements and industry standards. Participate in project planning, execution, and delivery to meet business objectives. Job Requirements Strong knowledge of Veeva EDC and its applications in clinical trials. Experience working in the IT Service & Consulting industry, prefe...

Minimum 8 years of experience in ETL development using SAS Data Integration Studio 4.9 ETL toolset. Skilled in various DI transformations including Look-up, Loop, Transpose, Sort, Append, Rank, List Data, Extract, Table Loader, Merger, Split, SQL, SCD Type 1 & Type 2 Loader, Data Validation, Creating Custom Transformations, Change Data Capture, managing indexes and constraints, using In-Database processing, verifying data quality settings, Importing SAS Code, Deploying & Scheduling Jobs, chaining jobs, metadata promotion Strong industry experience working in the data warehouse/BI arena including experience in data warehouse methodologies, including data management, data integration and analy...

Minimum 8 years of experience in ETL development using SAS Data Integration Studio 4.9 ETL toolset . Skilled in various DI transformations including Look-up, Loop, Transpose, Sort, Append, Rank, List Data, Extract, Table Loader, Merger, Split, SQL, SCD Type 1 & Type 2 Loader, Data Validation, Creating Custom Transformations, Change Data Capture, managing indexes and constraints, using In-Database processing, verifying data quality settings, Importing SAS Code, Deploying & Scheduling Jobs, chaining jobs, metadata promotion Strong industry experience working in the data warehouse/BI arena including experience in data warehouse methodologies, including data management, data integration and anal...

We are seeking an experienced SAS Administrator to join our team. As a SAS Admin, he/she will be responsible for the administration, maintenance, and support of our SAS platform. He/she will collaborate closely with stakeholders to ensure the SAS environment is optimized for performance, reliability, and security. Mandatory Skills SAS Admin

About the job Our Team: Sanofi Business Operations is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. Sanofi Business Operations strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally. 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 incl...

Our Team: Sanofi Business Operations is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. Sanofi Business Operations strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally. 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 datas...

We are looking for a skilled Senior Biostatistician and Statistical Programmer with 5 to 10 years of experience to join our team at Gratitude India Manpower Consultants Pvt. Ltd., located in [location to be specified]. The ideal candidate will have a strong background in biostatistics and statistical programming, with excellent analytical and problem-solving skills. Roles and Responsibility 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 delivery of high-quality results. Provide statistical guidance and support to ...

We are looking for a skilled Veeva EDC Clinical Programmer with 2 to 7 years of experience to join our team in Mumbai. The ideal candidate will have a strong background in IT Service & Consulting, particularly in clinical programming using Veeva EDC. Roles and Responsibility Design, develop, and implement clinical trial data management systems using Veeva EDC. Collaborate with cross-functional teams to ensure seamless integration of clinical data into the development process. Develop and maintain high-quality, accurate, and timely clinical trial data. Troubleshoot and resolve issues related to clinical data management and reporting. Ensure compliance with regulatory requirements and industry...

We are looking for a skilled Clinical SAS and SQL Programmer to join our team at Gratitude India Manpower Consultants Pvt. Ltd., with 2-5 years of experience in the IT Service & Consulting industry. Roles and Responsibility Design, develop, and implement clinical trial data management systems using SAS. Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Develop and maintain complex SQL queries for data extraction and analysis. Troubleshoot issues related to database performance and data integrity. Participate in code reviews to ensure adherence to coding standards. Stay updated with industry trends and emerging technologies in clinical trial data manag...

We are looking for a skilled R & SAS Data Analyst to join our team at Gratitude India Manpower Consultants Pvt. Ltd., with 2-5 years of experience in the IT Service & Consulting industry. Roles and Responsibility Analyze complex data sets using R and SAS tools to identify trends and patterns. Develop and implement data visualizations to communicate insights to stakeholders. Collaborate with cross-functional teams to design and implement data-driven solutions. Design and maintain databases to support business intelligence initiatives. Provide technical support and training to end-users on R and SAS tools. Develop and maintain documentation of data analysis processes and results. Job Requireme...

We are looking for a highly skilled and experienced Clinical Data Analyst and Programmer with expertise in SAS and Veeva to join our team at Gratitude India Manpower Consultants Pvt. Ltd. The ideal candidate will have 2-5 years of experience in the IT Service & Consulting industry. Roles and Responsibility Analyze and interpret complex clinical trial data using SAS. Develop and maintain databases, tables, and reports using Veeva. Collaborate with cross-functional teams to ensure accurate and timely delivery of projects. Design and implement data visualization tools to communicate insights to stakeholders. Ensure compliance with regulatory requirements and company standards. Provide technical...

We are looking for a skilled R + SAS Data Programming professional with 3 to 7 years of experience to join our team at Gratitude India Manpower Consultants Pvt. Ltd., located in the IT Service & Consulting industry. Roles and Responsibility Design, develop, and implement data programming solutions using R and SAS. Collaborate with cross-functional teams to identify business requirements and develop effective data models. Develop and maintain large-scale databases and data systems. Troubleshoot and resolve complex technical issues related to data programming. Provide training and support to junior team members on best practices and new technologies. Participate in code reviews and contribute ...

We are looking for a highly skilled and experienced Clinical Data Analyst and Programmer with expertise in SAS and Veeva to join our team at Gratitude India Manpower Consultants Pvt. Ltd. The ideal candidate will have a strong background in the IT Service & Consulting industry, specifically in clinical data analysis and programming. Roles and Responsibility Develop and maintain complex databases using SAS and Veeva. Analyze and interpret large datasets to identify trends and patterns. Design and implement effective data visualization techniques. Collaborate with cross-functional teams to ensure data quality and integrity. Develop and maintain technical documentation of data systems and proce...

We are looking for a skilled R + SAS Data Programming professional with 2 to 5 years of experience to join our team at Gratitude India Manpower Consultants Pvt. Ltd., located in the IT Service & Consulting industry. Roles and Responsibility Design, develop, and implement data programming solutions using R and SAS. Collaborate with cross-functional teams to identify business requirements and develop effective data models. Develop and maintain large-scale data systems, ensuring scalability and performance. Troubleshoot and resolve complex technical issues related to data programming. Provide technical guidance and support to junior team members. Participate in code reviews to ensure high-quali...

We are looking for a highly skilled and experienced Clinical Data Analyst and Programmer with expertise in SAS and Veeva to join our team at Gratitude India Manpower Consultants Pvt. Ltd. The ideal candidate will have a strong background in the IT Service & Consulting industry, specifically in clinical data analysis and programming using SAS and Veeva. Roles and Responsibility Develop and maintain complex databases and systems for clinical trial data management. Design, develop, and implement data models, data flows, and validation rules for clinical trial data. Collaborate with cross-functional teams to ensure accurate and timely delivery of high-quality results. Troubleshoot and resolve te...

Looking for a skilled Clinical Data Analyst and Programmer with expertise in SAS and Veeva to join our team. The ideal candidate will have 3-8 years of experience in the field. Roles and Responsibility Analyze and interpret complex clinical trial data using SAS. Develop and maintain databases, tables, and reports using Veeva. Collaborate with cross-functional teams to ensure accurate and timely delivery of results. Design and implement effective data management strategies. Ensure compliance with regulatory requirements and company standards. Provide technical support and training to junior team members. Job Requirements Strong knowledge of SAS programming language and its applications in cli...

Roles and Responsibility Design, develop, and implement clinical trial data management systems using SAS. Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Develop and maintain complex SQL queries for data extraction and analysis. Troubleshoot and resolve technical issues related to clinical trial data management. Ensure compliance with regulatory requirements and company standards. Participate in code reviews and contribute to improving overall code quality. Job Requirements Strong knowledge of SAS programming language and its applications in clinical trial data management. Experience with SQL querying languages such as SQL Server or Oracle. Familiar...

Roles and Responsibility Design, develop, and implement clinical trial protocols using SAS. Collaborate with cross-functional teams to ensure timely delivery of high-quality deliverables. Develop and maintain complex statistical analysis plans and datasets. Troubleshoot and resolve technical issues related to clinical trial data management systems. Participate in project meetings and provide input on project scope and timelines. Ensure compliance with regulatory requirements and company standards. Job Requirements Strong knowledge of clinical trial design principles and methodologies. Proficiency in SAS programming language, including Base SAS, Enterprise Guide, and Macros. Experience workin...

Roles and Responsibility Develop and implement statistical analysis plans for clinical trials, ensuring compliance with regulatory requirements. Collaborate with cross-functional teams to design and conduct statistical programming activities, including data management and reporting. Provide statistical expertise and guidance to junior staff members, promoting knowledge sharing and skill development. Conduct quality control checks on statistical deliverables, ensuring high standards of accuracy and attention to detail. Participate in project meetings and discussions, providing input on statistical aspects of projects and representing the views of stakeholders. Stay updated with industry trend...

Roles and Responsibility Design, develop, and implement clinical trial protocols using SAS. Collaborate with cross-functional teams to ensure timely delivery of high-quality deliverables. Develop and maintain complex statistical analysis plans and datasets. Troubleshoot and resolve technical issues related to clinical trial data management. Participate in project meetings and provide input on project scope and timelines. Ensure compliance with regulatory requirements and company standards. Job Requirements Strong knowledge of clinical trial design, protocol development, and statistical analysis. Proficiency in SAS programming language, including Base SAS and Proc SQL. Experience with clinica...

Roles and Responsibility Develop and implement statistical analysis plans for clinical trials. Design, analyze, and interpret complex data sets using statistical techniques. Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Provide expert guidance on statistical programming and analysis methodologies. Conduct quality control checks on statistical outputs and reports. Stay updated with industry trends and developments in statistical science. Job Requirements Strong knowledge of statistical concepts, including regression, time series, and mixed effects models. Experience with statistical software packages such as SAS or R. Excellent communication and in...