83 Clinical Sas Jobs

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,...

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.

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 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.

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 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.

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 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 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 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.

Role & responsibilities Job description: Location: Hyderabad, Corporate Office Job Type: Full-Time Collaborating with cross-functional teams (e.g., clinical researchers, medical experts, data scientists) to design clinical studies and research protocols. Developing statistical analysis plans (SAP), including the identification of primary and secondary endpoints, sample size calculations, and statistical methodologies. Ensuring statistical methods are aligned with regulatory requirements and industry standards, especially in clinical trials. Providing expertise on randomization techniques and adaptive designs. Leading the analysis of complex datasets, including data from clinical trials, epid...

The Clinical Data Coordinator (Intern/Fresher Level) plays a crucial role in ensuring the integrity and quality of clinical trial data. This position offers a valuable entry point into the field, providing hands-on experience in core data management tasks and industry best practices. Key Responsibilities: Data Entry and Verification: Meticulous data entry into electronic data capture (EDC) systems. Verify data accuracy and consistency against source documents (e.g., Case Report Forms). Learn to identify and flag potential data discrepancies. Query Generation and Resolution: Develop an understanding of data discrepancies and their underlying causes. Assist in generating data queries to clarif...

Hiring for No-1 IT MNC for Clinical SAS Programming Salary Up-to - 30LPA + NSA Any Grad/ PG With 5 Yrs Of experience In SDTM , ADAM , TLF , SAS MACROS CDISC standards etc Call @ WhatsApp- Shubhani - 8595849767 Call @ WhatsApp- Sejal -8595347527 Perks and benefits General Shifts Both Side Cabs Insurance etc

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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 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 dat...