409 Statistical Programming Jobs - Page 3

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4.0 - 9.0 years

3 - 7 Lacs

mumbai suburban

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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...

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4.0 - 9.0 years

3 - 7 Lacs

mumbai

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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...

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2.0 - 7.0 years

2 - 6 Lacs

bengaluru

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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...

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2.0 - 5.0 years

3 - 6 Lacs

bengaluru

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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 Enterprise Guide. Experience with...

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2.0 - 5.0 years

3 - 6 Lacs

navi mumbai

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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...

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3.0 - 8.0 years

8 - 12 Lacs

mumbai suburban

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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...

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2.0 - 5.0 years

3 - 6 Lacs

mumbai suburban

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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...

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3.0 - 8.0 years

8 - 12 Lacs

mumbai

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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...

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2.0 - 5.0 years

3 - 6 Lacs

mumbai

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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 solutions. Develop and maintain complex statistical analysis plans and programs. Troubleshoot and resolve technical issues related to clinical trial data management. Participate in project planning, execution, and monitoring activities. Ensure compliance with regulatory requirements and company standards. Job Requirements Strong knowledge of SAS programming language and its applications in clinical trial data management. Experience with statistical analysis plans and program development. Excellent problem-s...

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9.0 - 11.0 years

14 - 19 Lacs

navi mumbai

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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 reviews of clinical trial protocols, informed consent forms, and case report forms. Provide statistical input on study design, sample size calculations, and statistical methodologies. Conduct statistical review of protocol deviations and ensure timely resolution. Develop and maintain databases for tracking and managing statistical data from clinical trials. Prepare and present reports on statistical findings and recommendations to stakeholders. Job Requirements Master's degree...

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3.0 - 8.0 years

8 - 12 Lacs

navi mumbai

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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. Conduct statistical programming activities such as data management, reporting, and visualization. Ensure compliance with regulatory requirements and industry standards. Provide statistical guidance and support to junior team members. Job Requirements Strong knowledge of statistical concepts, methods, and techniques. Experience with statistical software packages such as SAS or R. Excellent analytical, problem-solving, and communicat...

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2.0 - 7.0 years

2 - 5 Lacs

mumbai

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Roles and Responsibility Design, develop, and implement clinical trial data management systems using CDMS. Collaborate with cross-functional teams to ensure seamless integration of clinical data into larger systems. Develop and maintain complex statistical analysis plans and reports using SAS. Troubleshoot and resolve issues related to clinical data management and reporting. Ensure compliance with regulatory requirements and industry standards for clinical trial data management. Provide technical support and training to end-users on CDMS and other clinical trial management systems. Job Requirements Strong proficiency in programming languages such as SAS and SQL. Experience working with CDMS ...

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2.0 - 7.0 years

2 - 6 Lacs

mumbai

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Roles and Responsibility Design, develop, and implement clinical SAS programs for data management and analysis. Collaborate with cross-functional teams to identify and prioritize project requirements. Develop and maintain complex SQL databases for data storage and retrieval. Write efficient and well-documented code using clinical SAS and SQL programming languages. Troubleshoot and resolve technical issues related to clinical SAS and SQL programming. Participate in code reviews to ensure high-quality deliverables. Job Requirements Strong knowledge of clinical SAS and SQL programming languages. Experience working in the IT Service & Consulting industry. Excellent problem-solving skills and att...

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3.0 - 7.0 years

3 - 6 Lacs

mumbai suburban

Work from Office

Roles and Responsibility Design, develop, and implement clinical data programming solutions using R/SQL. Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Develop and maintain complex databases and data systems. Troubleshoot and resolve technical issues related to clinical data programming. Ensure compliance with regulatory requirements and industry standards. Participate in code reviews and contribute to improving overall code quality. Job Requirements Strong knowledge of R/SQL programming languages. Experience working with large datasets and complex data systems. Excellent problem-solving skills and attention to detail. Ability to work collaborative...

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3.0 - 7.0 years

3 - 6 Lacs

mumbai

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Roles and Responsibility 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. Write efficient and well-documented code. Troubleshoot and resolve technical issues related to clinical data programming. Participate in code reviews and contribute to improving overall code quality. Job Requirements 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 and attention to detail. Ability to work coll...

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2.0 - 7.0 years

2 - 6 Lacs

navi mumbai

Work from Office

Roles and Responsibility Design, develop, and implement clinical trial data management systems using SAS and SQL. Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Develop and maintain complex statistical analysis plans and reports. Troubleshoot and resolve technical issues related to clinical trial data management. Ensure compliance with regulatory requirements and industry standards. Participate in project planning, execution, and monitoring activities. Job Requirements Strong knowledge of IT Service & Consulting, particularly in clinical programming using SAS and SQL. Experience working on clinical trials and data management projects. Excellent pro...

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2.0 - 7.0 years

2 - 6 Lacs

mumbai suburban

Work from Office

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 clinical trial data management systems. Ensure compliance with regulatory requirements and company standards. Participate in code reviews to improve overall quality of the codebase. 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. Familiarity with clinical tr...

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2.0 - 7.0 years

2 - 6 Lacs

hyderabad

Work from Office

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 management. Job Requirements Strong knowledge of SAS programming language and its applications in clinical trial data management. Proficiency in writing complex SQL queries for data extraction and analysi...

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2.0 - 7.0 years

2 - 5 Lacs

pune

Work from Office

Roles and Responsibility Design, develop, and implement clinical SAS programs for data management and analysis. Collaborate with cross-functional teams to identify business requirements and develop solutions. Develop and maintain complex SQL queries for data extraction and manipulation. Troubleshoot issues related to clinical SAS programs and provide technical support. Participate in code reviews and ensure adherence to coding standards. Stay updated with industry trends and emerging technologies in clinical SAS and SQL programming. Job Requirements Strong knowledge of clinical SAS programming language and its applications in data management and analysis. Experience with CDMS (Clinical Data ...

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2.0 - 5.0 years

3 - 6 Lacs

mumbai

Work from Office

Roles and Responsibility Design, develop, and implement clinical trial data management systems using SAS programming language. Collaborate with cross-functional teams to ensure timely delivery of high-quality deliverables. Develop and maintain complex statistical analysis plans and programs for clinical trials. Troubleshoot and resolve technical issues related to clinical trial data management systems. Participate in project meetings and provide input on project scope, timelines, and resource requirements. Ensure compliance with regulatory requirements and company standards for clinical trial data management. Job Requirements Strong knowledge of SAS programming language and its application i...

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2.0 - 7.0 years

2 - 6 Lacs

mumbai

Work from Office

Roles and Responsibility Design, develop, and implement statistical analysis software using R and SAS. Collaborate with cross-functional teams to identify business needs and provide data-driven solutions. Develop and maintain complex statistical models and algorithms. Troubleshoot and resolve technical issues related to R and SAS programming. Provide training and support to junior team members on R and SAS programming best practices. Stay updated with industry trends and emerging technologies in R and SAS programming. Job Requirements Strong proficiency in R and SAS programming languages. Experience working with large datasets and developing predictive models. Excellent problem-solving skill...

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2.0 - 7.0 years

2 - 6 Lacs

navi mumbai

Work from Office

Roles and Responsibility Design, develop, and implement statistical models using R and SAS. Collaborate with cross-functional teams to identify business problems and provide solutions. Develop and maintain large-scale data systems and databases. Write efficient and well-documented code. Troubleshoot and resolve technical issues. Participate in code reviews and contribute to improving overall code quality. Job Requirements Strong knowledge of R and SAS programming languages. Experience working with large datasets and databases. Excellent problem-solving skills and attention to detail. Ability to work collaboratively in a team environment. Strong communication and interpersonal skills. Familia...

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5.0 - 9.0 years

9 - 14 Lacs

hyderabad

Work from Office

Description Manager Statistical Programming Syneos Healthis a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities Our Clinical Development model brings the customer and the patient to the center of everything that we do We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem solvers, inno...

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4.0 - 7.0 years

7 - 12 Lacs

hyderabad

Work from Office

Description Sr Statistical Programmer Syneos Healthis a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities Our Clinical Development model brings the customer and the patient to the center of everything that we do We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem solvers, innovating...

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7.0 - 12.0 years

5 - 9 Lacs

hyderabad

Work from Office

Main responsibilities: Use statistical, analytical, data management and computational skills to execute analyses of pre-existing data to investigate research questions in teamwork with colleagues from GenMed, medical affairs, business operations & strategy (BO&S) and commercial product teams; Work together with these SGz functions and the RWE group located in the Chief Digital Office that maintains Sanofi data assets via primary data collection, license of secondary data sources, and de-identified clinical trial data; Require a strong background in statistics, statistical programming, observational research design, and experience in the pharmaceutical industry People: (1) Work together with ...

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