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9.0 - 12.0 years
8 - 12 Lacs
navi mumbai
Work from Office
Roles and Responsibility Develop and implement statistical analysis plans for clinical trials. Collaborate with cross-functional teams to ensure timely and accurate data delivery. Conduct statistical reviews of case report forms, annotated CRFs, database structures, and study-related documentation. Provide statistical input into protocol development and review. Ensure compliance with regulatory requirements and company policies. Mentor junior statisticians and provide guidance on statistical methodologies. Job Requirements Strong knowledge of statistical concepts, including regression, time series, mixed effects, and survival analysis. Experience with statistical software packages such as SA...
Posted 1 week ago
2.0 - 7.0 years
5 - 9 Lacs
bengaluru
Work from Office
Using a commercial industry perspective to advise clients on advanced practices, typical industry approaches, market behavior. Developing quantitative financial models for commodity and financial contracts, including implementing market factor simulation techniques and a variety of stochastic and numerical methods Using and enhancing proprietary valuation models, including the selection of appropriate inputs and techniques Leveraging machine learning techniques and statistical programming packages to perform analysis on commodity instruments Presenting results, both internally and externally, including using modern data visualization tools Writing client reports describing work performed, co...
Posted 1 week ago
7.0 - 10.0 years
25 - 30 Lacs
pune
Work from Office
Description Assoc Dir, Statistical Prog 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, innovati...
Posted 1 week ago
7.0 - 10.0 years
25 - 30 Lacs
pune
Work from Office
Description Assoc Dir, Statistical Prog 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, innovati...
Posted 1 week ago
10.0 - 14.0 years
14 - 18 Lacs
gurugram
Work from Office
As the Data Science Manager for the Life Science Research & Development team, you'll lead your team to create data-driven solutions using ML algorithms. You'll educate teams on machine learning models and help turn goals into data solutions. You will be responsible for applying analytical techniques to model complex business problems, uncovering insights, and identifying opportunities using statistical, algorithmic, mining, and visualization techniques. In addition to advanced analytics skills, the candidate should also be skilled in integrating and preparing large, varied datasets, implementing specialized database and computing environments, and communicating results. This role requires a ...
Posted 1 week ago
2.0 - 4.0 years
4 - 6 Lacs
bengaluru
Work from Office
Are you ready to make a difference in the world of biopharmaceuticalsAs a Statistical Programmer II, youll play a crucial role in developing and validating programs that create datasets conforming to Alexion and CDISC standards. Your work will be pivotal in generating Tables, Listings, and Figures for analysis purposes, ensuring adherence to ICH guidelines, Good Clinical Practices, and regulatory requirements. Youll be part of a dynamic team, contributing to moderate scope and medium complexity studies or drug projects. With guidance from experienced programmers, youll have the opportunity to enhance your skills in SAS programming and statistical concepts while collaborating across functions...
Posted 1 week ago
4.0 - 9.0 years
3 - 7 Lacs
pune
Work from Office
Analyze and interpret complex clinical data using SAS. Develop and maintain databases, data systems, and computer models for clinical trial management. Collaborate with cross-functional teams to design and implement data analysis plans. Ensure data quality, integrity, and compliance with regulatory requirements. Provide technical support and training to junior staff members on data analysis tools and techniques. Participate in project meetings and contribute to the development of project plans and timelines. Job Requirements Strong knowledge of SAS programming language and its applications in clinical data analysis. Experience with Veeva or similar clinical trial management systems. Excellen...
Posted 1 week ago
2.0 - 7.0 years
2 - 6 Lacs
mumbai
Work from Office
Design, develop, and implement clinical trial data management systems using SAS. Collaborate with cross-functional teams to ensure seamless integration of clinical data into existing systems. Develop and maintain complex SQL queries to extract insights from large datasets. Troubleshoot issues related to clinical trial data management and reporting. Ensure compliance with regulatory requirements and industry standards. Participate in code reviews and contribute to improving overall code quality. Job Requirements Strong proficiency in SAS programming language, including Base SAS and Enterprise Guide. Experience with SQL programming, particularly in a clinical trial context. Knowledge of clinic...
Posted 1 week ago
3.0 - 6.0 years
3 - 7 Lacs
pune
Work from Office
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. Participate in code reviews and contribute to improving overall code quality. Stay up-to-date with industry trends and emerging technologies in Veeva EDC clinical programming. Job Requirements Strong understanding of Veeva EDC clinical programming principles and practices. Proficiency in developing complex programs using Veeva EDC tools and te...
Posted 1 week ago
3.0 - 8.0 years
8 - 12 Lacs
bengaluru
Work from Office
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 junior staff members. Participate in project meetings and contribute to the development of project plans. Ensure compliance with regulatory requirements and company standards. Job Requirements Strong knowledge of biostatistics and statistical programming principles. Experience with statistical software packages, such as SAS or R. Excellent analytical and problem-solving skills, with attentio...
Posted 1 week ago
2.0 - 7.0 years
2 - 5 Lacs
mumbai
Work from Office
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. Expertise in SQL programming for data extraction and manipula...
Posted 1 week ago
2.0 - 7.0 years
2 - 5 Lacs
mumbai suburban
Work from Office
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 to ensure high-quality deliverables. 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 SQL programming languages, including query design ...
Posted 1 week ago
2.0 - 7.0 years
2 - 5 Lacs
navi mumbai
Work from Office
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 programming and provide technical support. Participate in code reviews and contribute to improving overall code quality. Stay updated with industry trends and emerging technologies in clinical SAS programming. Job Requirements Strong knowledge of clinical SAS programming and SQL. Experience working with CDMS is essential. Excellent problem-solving skills and attention to detail. Ability to ...
Posted 1 week ago
3.0 - 8.0 years
8 - 12 Lacs
mumbai
Work from Office
Roles and Responsibility Develop and implement statistical analysis plans for clinical trials. Conduct data review and quality control checks to ensure accuracy and completeness. Collaborate with cross-functional teams to design and execute statistical protocols. Provide statistical guidance and support to junior staff members. Review and approve statistical deliverables such as reports and presentations. Stay up-to-date with industry trends and developments in biostatistics and statistical programming. Job Requirements Strong knowledge of biostatistics and statistical programming principles. Experience working with clinical trial data and statistical software packages. Excellent analytical ...
Posted 1 week ago
4.0 - 9.0 years
3 - 7 Lacs
mumbai
Work from Office
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...
Posted 1 week ago
3.0 - 6.0 years
3 - 7 Lacs
mumbai
Work from Office
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...
Posted 1 week ago
3.0 - 6.0 years
3 - 7 Lacs
mumbai
Work from Office
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...
Posted 1 week ago
3.0 - 6.0 years
3 - 7 Lacs
navi mumbai
Work from Office
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 &...
Posted 1 week ago
9.0 - 12.0 years
8 - 12 Lacs
mumbai
Work from Office
Roles and Responsibility Develop and implement statistical analysis plans for clinical trials. Conduct data review and quality control checks to ensure accuracy and compliance with regulatory requirements. Collaborate with cross-functional teams, including medical writing, biostatistics, and project management. Provide statistical guidance and support to junior staff members. Participate in developing and implementing new statistical methodologies and technologies. Ensure timely delivery of high-quality results and meet project deadlines. Job Requirements Strong knowledge of statistical concepts, including regression, time series, and mixed effects models. Experience with statistical softwar...
Posted 1 week ago
3.0 - 6.0 years
3 - 7 Lacs
mumbai suburban
Work from Office
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...
Posted 1 week ago
4.0 - 9.0 years
7 - 11 Lacs
hyderabad
Work from Office
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...
Posted 1 week ago
3.0 - 6.0 years
3 - 7 Lacs
bengaluru
Work from Office
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...
Posted 1 week ago
2.0 - 7.0 years
2 - 6 Lacs
pune
Work from Office
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...
Posted 1 week ago
4.0 - 9.0 years
3 - 7 Lacs
bengaluru
Work from Office
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...
Posted 1 week ago
4.0 - 9.0 years
3 - 7 Lacs
navi mumbai
Work from Office
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...
Posted 1 week ago
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