83 Clinical Sas Jobs - Page 4

Job Title: Clinical SAS Programmer Career Level: CL11 (3+ years) / CL10 (5+ years) Domain: Life Sciences Location: Koramangala, Bangalore Work Mode: Work from Office (No WFH) Shifts: Flexible / Rotational Job Description: We are looking for experienced Clinical SAS Programmers to join our Life Sciences team. The ideal candidate will have strong hands-on experience in Clinical SAS, including Macros and Proc SQL, and a solid understanding of clinical trial processes. Key Responsibilities: Perform data analysis using SAS programming techniques as per project requirements. Develop and maintain SAS Macros and programs using Proc SQL. Work with clinical trial data to support statistical analysis a...

Should have 3+ experience in Clinical SAS.experience in Macros & ProcSQLknowledge of clinical trials.work in Shift.No WFH.Education Life Science Graduates( Bpharm, Mpharm, Pharm D, Bsc ( Biotechnology), BE (Biotechnology).Domain:Life Science

Hi , WE are hiring for Leading ITES Company for SAS Programmer & CDB Programmer ( J Reviewer/Python/SAS) Role & responsibilities: 1.Create data cleaning reporting solutions study status metric, and monitoring reports and visualizations required per standard and study specific data review plans. 2. Develop library of reusable checks working closely with data engineers and config specialists. 3. Collaborate with cross functional teams in creating business rules and automated check library across TAU. 4. Serves as a technical resource for creating data analytics to help with data validation and cleaning. 5. Provide programming expertise for data cleaning to efficiently ensure high quality data....

Hi We are hiring for Leading ITES Company for SAS+R Programmer Profile. Role & responsibilities: a) Any Graduate b) Minimum of 3 years of experience in SAS + R programming c) Familiarity with data visualization techniques and tools in R d) CDISC knowledge & experience Roles & Responsibilities: Create data cleaning reporting solutions, study status metric, and monitoring reports and visualizations required per standard and study specific data review plans. Contribute to process improvements and development of programming standards using R. Minimum of 3 years of experience in R programming including familiarity with R packages (e.g., Tidyverse, ggplot2, survival) Familiarity with data visualiz...

Hi, We are hiring for ITES Company for SDTM Programmer Role. Job description: Minimum 2 years of experience for Senior Statistical programming is a mandate. • Having strong understanding of SAS Base/Macros/GTL and experience of SDTM/ADAM/TLFs creation as per CDISC standards. • Associate should be able to manage communication with customers, track and ensure quality on-time deliverables • Implementation of process improvements for enhanced quality and efficiency gains, institute robust processes to ensure consistent outcomes with quicker turn-around time. • Experience in SDTM, ADAM & TLF • Experience in EDC & VEEVA • Expertise in Base and Advance SAS programming. • Expertise in developing mac...

Hi, We are hiring for the ITES Company for the Clinical SAS + SQL Programmer Profile. Job Description: Minimum 4 years of experience in any CDMS application. To perform a wide range of Clinical Data Management activities resulting in high quality database within stipulated timelines. To provide expertise in programming concepts to the Data Management team Must be able to develop the connection with the stake holders by pro-actively communicating over the calls and handling the queries by resolving them on the spot or later depending on the nature of the problem. Must be able to contribute the solutions to the DMs or Medical scientist for their New requirements either programmatically or conv...

Clinical SAS Programmer Location: Bangalore Experience: 3+ years Notice Period: Immediate Joiners to 1 month Preferred Skills:Clinical SAS, Proc SQL, SAS MACROS, Clinical trials, SDTM, ADAM 5 days of WFO and 2 days fixed week off 2 way cab upto 35km

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...