83 Clinical Sas Jobs - Page 2

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 statistical analysis plans and programs. Troubleshoot and resolve technical issues related to clinical trial data management. Ensure compliance with regulatory requirements and company standards. Participate in project planning, execution, and reporting activities. Job Requirements Strong knowledge of SAS programming language and its applications in clinical trial data management. Experience working with large datasets and developing complex statistical analysis plans. ...

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...

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...

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 ...

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 ...

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...

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. 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...

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 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 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...

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 ...

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...

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...

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...

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...

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 ...

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...

**Greetings from You & I Consulting!** We've proudly helped candidates build careers at 64+ top MNCs across India, and were excited to bring you a new opportunity with a leading global company. If you have experience in Statistical Programming, this role is your next step forward! Senior Lead Statistical Programmer!!! We are hiring for: Senior Lead Statistical Programmer up to 22LPA ctc **To Apply Call on Puja- 8167854231 /Or Whatsapp on the same Number with your CV** Experience Level: 4 to 18 years Location-Mumbai , Kochi, Bangalore and PAN India Job Description : We are seeking an experienced and driven Senior Lead Statistical Programmer with 1015 years of experience in clinical trial prog...

You should have 4 to 5 years of experience in SAS/STAT, SAS Data Management, SAS, and Base SAS. As the ideal candidate, you will possess a strong background in Statistical Programming and Biostatistics. Your role will involve leading the team in developing and implementing statistical programming solutions using SAS/STAT, SAS Data Management, and Base SAS. You will also be responsible for overseeing the creation and validation of datasets, tables, listings, and figures for clinical trials. This position requires expertise in Clinical SAS and Power BI within the Pharmaceutical industry. The role falls under the category of Life Sciences and Pharma, and it is a full-time, permanent employment ...

Openings for Statistical Programmer - Band - 4/5/6 Salary Up-to - 30 LPA + VAriables Any Grad / PG with - 5 yrs of exp Clinical SAS , Creation & Validation of ISS & ISE reports Development of sas macros etc Call @ WhatsApp- Shubhani -8595849767

Position Overview : We are seeking a skilled Statistical Programmer to join our clinical research team. The successful candidate will be responsible for programming, validating, and delivering statistical outputs for clinical trials while ensuring compliance with regulatory standards and industry best practices. Key Responsibilities : Programming & Data Management : - Develop and maintain SAS programs for clinical trial data processing, analysis, and reporting. - Map clinical trial data to CDISC standards (SDTM and ADaM) ensuring compliance with regulatory requirements. - Create and maintain analysis datasets following CDISC implementation guidelines. - Perform data validation and quality co...

In this role you will be part of our Centre of Excellence team working specifically in SDTM therefore extensive experience and knowledge is required in this area. What you'll be doing: Develops SAS programs to generate listings, tables and figures as outlined by mock TLF shells Performs quality control (source code review, double-programming and log review) of SAS programs Develops SAS programs to generate CDISC and other analysis data sets as outlined by respective specifications Prepares specifications for CDISC and other analysis data sets Assists Data Management with SAS programming needs Acts as Lead Biostatistical Programmer to interact with the Lead Biostatistician and the study team ...

About The Role Skill required: Clinical Data Services - Clinical Database Programming Designation: Clinical Data Svs Associate Qualifications: BE/BTech/BCA Years of Experience: 1 to 3 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do You will be part of our Life Sciences R...

Skill required: Clinical Data Services - Clinical Reports Management Designation: Clinical Data Svs Associate Qualifications: BE/BTech/Masters in actuarial science Years of Experience: 1 to 3 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do You will be part of our Life Sc...