Sas programmer • india
We are looking for experienced.Statistical Programming professionals.Statistical Programming Consultant / Senior Statistical Programmer.Bachelor's degree in Statistics, Biostatistics, Mathematics, ... Show more
Job title: Senior Principal Statistical Programmer – Clinical SAS Reports to: Vice President - Operations Job purpose To lead the programming, validation, and delivery of high-quality statistica... Show more
Prepared Functional Design Documents (FDD), Detailed Design Documents (DDD), Software Configuration Plans (SCP), and Unit Test Plans (UTP) to support project delivery and compliance requirements.De... Show more
Location & Type (Hybrid/Onsite/Remote):.Adherence to all department-specific and project standards and SOPs.Perform all responsibilities associated with SAS� Programmer roles.Assist the Programmers... Show more
Job Title: Senior Specialist, Clinical Trials - SAS programming.Department: Biostatistics and SAS Programming.At Syngene, safety is at the heart of everything we do personally and professionally.Sy... Show more
Job Title / Primary Skill: SAS Programmer.Looking for immediate to shorter notice period.Develop, validate, and maintain SAS programs for clinical study deliverables.Generate and review Data Valida... Show more
Experience (in years): 5-10 years.Education: Bachelor's/Master's in Statistics, Computer Science,Maths, Life Sciences, or related field or any other related discipline.Proficiency in SAS, SAS Macro... Show more
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based SAS Programmer to join our Biostatistics team in India, Mumbai.This position will work on a team... Show more
The SAS Administrator, specializing in SAS administration will be part of the organization's Professional Services team in India, which provides implementation services, business consulting, IT ser... Show more
Clinical SAS Programmer / Senior Clinical SAS Programmer.Strong hands-on ADaM Programming.Safety and Efficacy Programming.Independent/Scratch Programming.End-to-End Clinical Trial Experience (Phase... Show more
We are looking for an experienced.Clinical SAS Programmer / SAS BI Engineer.CDISC standards, and regulatory submission deliverables.The ideal candidate should have hands-on experience in.Develop an... Show more
We are looking for candidates with strong hands-on experience in:.End-to-End SAS Programming in Clinical Trials.Good understanding of Tumor Assessments and RECIST Guidelines.Experience developing S... Show more
Advanced Clinical is a clinical development and strategic resourcing organization committed to providing a better clinical experience across the drug development journey.Our goal is to improve the ... Show more
Develop and validate SDTM domains for assigned studies.Generate SDTM validation reports and Pinnacle 21 compliance outputs.Prepare SDTM Reviewer's Guide and related support documents.Create analysi... Show more
Provide Statistical Programming support for clinical trial projects.Develop, validate, and maintain SAS programs and outputs for the management, analysis, and reporting of clinical trial data.Devel... Show more
Company Name : Willware Technologies.Building and maintaining the Bank's business data marts and data assets that will drive the BI,.Regulatory Reporting and Analytics activities for the organizati... Show more
We are looking for an experienced SAS Programmer.Profile is required to join on immediate/Urgent participation.Job Description & Key Responsibility.Good exposure in SAS Base, Macro, SQL.Experience ... Show more
Project Role: Clinical SAS Programmer Work Experience: 5+ Years Work location: Any IQVIA office Location In India Work Mode: Hybrid Must Have Skills: Clinical SAS/DM SAS/SAS Macros , Listing an... Show more
Develop custom software solutions to design, code, and enhance components across systems or applications.Use modern frameworks and agile practices to deliver scalable, high-performing solutions tai... Show more
Hiring: SAS Developer | 5–8 Years Experience.SAS Programming, SQL/ETL, SAS Migration, and Azure Data Engineering.SAS migration projects using migration accelerators.Develop, enhance, optimize, and ... Show more
We are looking for experienced Statistical Programming professionals to join our team and support clinical development, analysis, and regulatory submission activities.
Positions: Statistical Programming Consultant / Senior Statistical Programmer
Experience:
• Consultant: 4–6 years
• Senior: 6–8 years
Education: Bachelor's degree in Statistics, Biostatistics, Mathematics, Computer Science, Life Sciences, or related field
Key Skills & Responsibilities:
• Strong hands-on experience in SAS / Clinical Statistical Programming
• Develop SAS programs for ADaM datasets, Tables, Listings & Figures (TLFs)
• Perform programming validation and ensure quality of datasets and outputs
• Strong understanding of CDISC standards, SDTM, ADaM, and clinical data structures
• Experience with clinical data processing, including eDC, SDTM, and upstream data sources
• Generate downstream deliverables including ADaM, Data Definition Tables, and e-submission packages
• Support regulatory submissions and review submission-related deliverables
• Review and interpret Statistical Analysis Plans (SAPs) and other clinical planning documents
• Work with vendors on programming standards, specifications, conventions, and data transfers
• Ensure compliance with regulatory requirements, SOPs, and industry standards
• Experience with Pinnacle 21, XML, relational databases, and MS Office
• Strong understanding of clinical trials, statistical terminology, medical terminology, and protocol design
Good to Have:
• Experience supporting NDA, BLA, MAA, or other regulatory filings
• Knowledge of the drug development process and global regulatory requirements
• Experience with R
• Exposure to Linux/Unix environments
Interested candidates Share your updated resume to [HIDDEN TEXT] or apply through LinkedIn.
Skills Required
cdisc standards , protocol design , Relational Databases, Sdtm, Ms Office, Xml, EDC, Medical Terminology, Regulatory Submissions, Sas, Linux, Unix
