Senior Clinical Statistical Programmer in Chennai, भारत
VUEVERSE CONSULTING SERVICES
Chennai, भारत
Job Title : Sr. SAS ProgrammerLocation : Hyderabad/Bangalore/Chennai/PuneWork Mode : Work from Office (5 days a week)Job Type : Full timeEssential Duties and Responsibilities : As a Sr. SAS Programmer, you will be creating, validating, and maintaining statistical programs and datasets used in regulatory https://jobeax.com/link/2NzhJumMgHZavEHq Responsibilities : Develop and validate SAS Macro's/programs for : - Data cleaning and transformation- Analysis datasets (ADaM)- SDTM datasets (Study Data Tabulation Model)- Generate Tables, Listings, and Figures (TLFs)- Ensure compliance with CDISC standards (SDTM, ADaM) & Regulatory guidelines (FDA, EMA)- Perform quality checks and validation of outputs- Collaborate with other stakeholders like Biostatisticians & Clinical data management teams- Support submission packages for regulatory authoritiesRequired Skills : - Strong proficiency in Base SAS, SAS/STAT, SAS Macros- Experience with CDISC standards (SDTM & ADaM)- Knowledge of Clinical trial processes & Good Clinical Practice (GCP)- Familiarity with Regulatory submissions (eCTD)- Good analytical and problem-solving skillsQualifications : - Bachelors or Masters degree in Statistics / Biostatistics, Computer Science or Life Sciences- Typically 5 - 12 years of SAS programming experience (varies by level)Preferred Qualifications : - Experience in pharmaceutical or CRO industry- Exposure to tools like SAS, R & Python- Prior work on submission projects (ref:hirist.tech)
About the Role We're hiring an experienced Statistical Programmer with expertise in Clinical SAS Programming, CDISC Standards, ADaM, SDTM, Tables, Listings & Figures (TLF/TFL), Clinical Data Analysis, and Regulatory Submissions . This opportunity is ideal for professionals with experience supporting clinical trials, drug ...
At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters.
Senior Statistical Programmer leading SAS programming for clinical trial data management and regulatory submissions. Develops CDISC datasets, mentors junior staff, and ensures compliance with regulatory standards across complex studies. Responsibilities - Develop, test, and execute SAS programs for CDISC-compliant datasets ...
Senior Statistical Programmer leading SAS programming for clinical trial data management and regulatory submissions. Develops CDISC datasets, mentors junior staff, and ensures compliance with regulatory standards across complex studies. Responsibilities - Develop, test, and execute SAS programs for CDISC-compliant datasets ...
... also ensure compliance with ICH guidelines, Good Clinical Practices, and regulatory requirements. They will support the Programming Lead and may represent Statistical Programming in meetings with internal and external clients and cross-functional project teams. The Senior Statistical Programmer will act as a mentor to Statistical ...
... documents. - Lead the development of standard SAS macros and contribute to standard operating procedures. - Provide oversight, mentoring, and guidance to Statistical Programmers, Statistical Analysts, and Senior Statistical Analysts. - Support statistical analyses and clinical study programming activities. - Collaborate ...
... career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. The Associate Statistical Programmer is responsible for creating, validating, and executing statistical programs to generate analysis datasets, tables, figures, listings, and safety ...
Associate Statistical Programmer at ICON in Bangalore responsible for developing, validating, and executing statistical programs to produce analysis datasets, tables, figures, and safety outputs for clinical trials. Requires 0-2 years of R programming experience with basic SAS knowledge and a Master's or Bachelor's degree ...
... SAS macros and contribute to standard operating procedures. - Provide technical oversight and mentoring to Statistical Programmers, Statistical Analysts, and Senior Statistical Analysts. - Collaborate effectively with Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations ...
... and contribute to standard operating procedures. - Provide technical guidance, mentoring, and oversight to Statistical Programmers, Statistical Analysts, and Senior Statistical Analysts. - Collaborate with statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing, and Clinical Operations teams. - Support ...
Johnson & Johnson seeks an experienced statistical programmer to support clinical trial data analysis and reporting activities. The role involves designing and developing programs for clinical research, ensuring CDISC compliance, and collaborating with cross-functional teams on trials of low to medium complexity. Responsibilities ...