544 Statistical Programming Jobs

We are seeking a proactive and detail-oriented Site Solution Executive to support and coordinate all clinical trial activities at the site in accordance with GCP guidelines , protocol requirements , and local regulatory standards . In this role, you will work closely with the Principal Investigator (PI) , site study team , and sponsor representatives to ensure efficient execution of clinical trials, compliance with study timelines, and high-quality data management. This is an excellent opportunity for professionals passionate about clinical research, site operations, and patient safety. Key Responsibilities: Coordinate and facilitate all clinical trial activities at the site , ensuring compl...

We are looking for a skilled Lead R&D Technologist to join our Statistical Programming team in India. The ideal candidate will have 4 to 8 years of experience in the field. Roles and Responsibility Develop and implement statistical programming solutions for complex data analysis projects. Collaborate with cross-functional teams to design and execute experiments and studies. Design, develop, and maintain SAS programs for data manipulation and analysis. Troubleshoot and resolve technical issues related to statistical programming. Mentor junior team members and provide guidance on best practices. Participate in project planning, prioritization, and resource allocation. Job Requirements Strong k...

Primary Job Function Responsible for the integrity of the programming/computing solutions for multiple clinical trials (or equivalent) and/or publication activities. In collaboration with the Biostatistician and Senior Programmer, provide programming support to project-level programming deliverables and other adhoc programming requests. Roles and Responsibilities Ensure understanding and compliance with study and project programming standards. Responsible for development of programming specification. Create and Validate Safety and Efficacy Analysis Datasets in adherence with CDISC and client specific standards and maintain quality and accuracy. Create and Validate Safety and Efficacy Tables,...

Develop and implement statistical analysis plans for clinical trials.Conduct statistical programming activities, including data management, reporting,visualization.Collaborate with cross-functional teams to ensure timely and accurate delivery Required Candidate profile Strong knowledge of biostatistics and statistical programming principles and practices.Experience with statistical software packages, such as SAS or R.Excellent analytical, problem-solving

Develop and implement statistical analysis plans for clinical trials.Conduct statistical reviews of case report forms, annotated CRFs, database structures, and study-related documentation.Collaborate with cross-functional teams to ensure timely Required Candidate profile Strong understanding of biostatistics principles and methodologies.Experience working with clinical trial data and statistical software packages.Excellent communication and interpersonal skills.

Design, develop, and implement Veeva EDC clinical programming solutions.Collaborate with cross-functional teams to ensure seamless integration of EDC systems.Develop/ maintain technical documentation for EDC systems.Troubleshoot and resolve issues Required Candidate profile Strong understanding of Veeva EDC clinical programming principles and practices.Experience working with various EDC tools and technologies.Excellent problem-solving skills and attention to detail.

Design, develop, and implement Veeva EDC clinical programming solutions.Collaborate with cross-functional teams to ensure seamless integration of EDC systems.Develop and maintain high-quality code that meets industry standards. Required Candidate profile Strong understanding of Veeva EDC clinical programming principles and practices.Experience working with various EDC systems and technologies.Excellent problem-solving skills and attention to detail.

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. Required Candidate profile 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

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. 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 implement statistical analysis plans for clinical trials.Conduct statistical programming activities, including data management, reporting, visualization.Collaborate with cross-functional teams to ensure timely delivery of high-quality Required Candidate profile Strong knowledge of biostatistics and statistical programming principles and practices.Experience with statistical software packages, such as SAS or R.Excellent analytical, problem-solving,

Design, develop, and implement Veeva EDC clinical programming solutions.Collaborate with cross-functional teams to ensure seamless integration of EDC systems.Develop and maintain high-quality code, adhering to industry standards and best practices. Required Candidate profile Strong understanding of Veeva EDC clinical programming principles and methodologies.Proficiency in developing complex programs using Veeva EDC tools and technologies.Excellent problem-solving skills

Analyze and interpret complex clinical trial data using SAS.Develop and maintain databases, spreadsheets, and reports using Veeva.Collaborate with cross-functional teams to ensure accurate and timely delivery of results. Required Candidate profile Strong proficiency in SAS programming language.Experience with Veeva database management system.Excellent analytical and problem-solving skills.Ability to work independently and as part of a team.

Develop and maintain complex statistical models and data visualizations using SAS.Collaborate with cross-functional teams to design and implement data-driven solutions.Analyze large datasets to identify trends and patterns Required Candidate profile Strong proficiency in SAS programming language, including Base SAS and Enterprise Guide. Experience with statistical modeling techniques, such as regression and time series forecasting.

Design, develop, and maintain complex statistical analysis systems using SAS.Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Required Candidate profile Strong knowledge of SAS programming language and its applications in clinical trial data management. Experience with SQL database management systems and querying languages.

Design, develop, and maintain complex statistical analysis systems using SAS.Collaborate with cross-functional teams to ensure timely delivery of high-quality results.Develop and implement efficient data processing Required Candidate profile Strong knowledge of SAS programming language and its applications in clinical trial data management. Experience with SQL programming language and database management systems.

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.

Design, develop, and implement clinical trial data management systems using CDMS expertise.Collaborate with cross-functional teams to ensure seamless integration of clinical data management systems. Required Candidate profile Strong understanding of clinical trial data management principles and practices. Proficiency in CDMS, SAS programming language, and SQL database management systems.

Develop and maintain databases, spreadsheets, and reports for tracking and analyzing clinical trial data.Collaborate with cross-functional teams to ensure accurate and timely delivery of high-quality results. Required Candidate profile Strong knowledge of SAS programming language and its applications in clinical trial data analysis. Experience with Veeva or similar systems is desirable.

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 proficiency in 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 clinical trial data management systems using SAS.Develop and maintain databases for clinical trial data, ensuring data quality and integrity.Collaborate with cross-functional teams Required Candidate profile Strong knowledge of SAS programming language, including Base SAS and Enterprise Guide. Experience with clinical trial data management, statistical analysis, and database development.

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. Required Candidate profile 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

Design, develop, and maintain clinical data systems using R/SQL.Collaborate with cross-functional teams to ensure data quality and integrity.Develop and implement data validation and verification processes. Required Candidate profile Strong knowledge of R/SQL programming languages. Experience working with clinical data systems and databases. Understanding of data modeling and data warehousing concepts.

Design, develop, and maintain complex statistical analysis systems using SAS.Collaborate with cross-functional teams to ensure timely delivery of high-quality results.Develop and implement data validation and quality control processes Required Candidate profile Strong knowledge of SAS programming language and its applications in clinical trial data management. Experience with SQL database management systems and data analysis tools.

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

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.