Senior Statistical Programmer I in Bangalore, India - Jobeax
Vacancy description
Senior Statistical Programmer I in Bangalore, भारत
AstraZeneca
HybridMix of office and remote
Bangalore, भारत
Senior Statistical Programmer role supporting oncology clinical development at AstraZeneca's Bangalore office. Responsibilities include statistical programming for clinical study reports, regulatory submissions, and data analysis across the drug development pipeline. Hybrid work arrangement with science-focused pharmaceutical organization.
Responsibilities
Develop clinical study reports and support regulatory submissions for oncology programs
Provide statistical programming support for analysis and reporting at study level
Lead or contribute to concurrent programming activities across clinical development projects
Ensure compliance with technical and regulatory requirements in data programming
Collaborate with global biometrics and clinical teams on drug development initiatives
Requirements
Bachelor's or Master's in Mathematics, Statistics, Computer Science, or Life Sciences
3+ years industry experience with Master's degree, or 5+ years with Bachelor's
Advanced SAS programming expertise in clinical drug development
Knowledge of CDISC standards and regulatory requirements in pharmaceuticals
Strong attention to detail and ability to manage concurrent studies
Excellent verbal and written communication skills
Experience leading clinical trial studies or activities preferred
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 ...
Senior Statistical Programmer 2 role at a global CRO involves leading programming initiatives, developing and validating clinical datasets using SAS, and providing consultancy on CDISC standards and regulatory submissions. The position requires mentoring team members and driving continuous improvement across biostatistical ...
... interact with each other, customers, patients and suppliers. As a Statistical Programmer II at ICON, you will the development, validation, and execution of statistical programs to support clinical trial analysis and reporting. What You Will Do: - Developing, validating, and maintaining complex statistical programs (SAS, ...
IQVIA seeks a Statistical Programmer 2 to develop analysis plans, write detailed specifications, and author statistical study report sections. The role involves mentoring junior staff, leading biostatistical teams on assigned studies, and ensuring high-quality deliverables aligned with clinical trial standards. Responsibilities ...
Key Purpose : The Senior SAS programmer leads the programming activities for various purposes includingCSRs, DSMBs, interim analyses, manuscripts, etc. Mainly supports statistical programming of statistical analysis plan (SAP)-planned tables, data listings, and graphs for CSRs, as well as integrated summaries of safety ...
Amgen seeks a Biostatistical Programming Manager to lead statistical programming teams and serve as Study Lead Programmer for clinical trials in Hyderabad, India. The role involves managing end-to-end study programming, establishing standards and timelines, and supporting regulatory submissions across integrated analyses. ...
IQVIA seeks a Manager Statistical Programmer to lead a team in Bangalore, overseeing hiring, training, and resource allocation across multiple clinical research projects. The role combines management responsibilities with technical expertise in statistical programming and clinical development processes. Responsibilities ...
... Mathematics, Statistics, Engineering, Computer Science/Applications, Pharmacy, or any other similar type of qualification- At least six years (Lead)/Four years (Senior) of Clinical SAS programmer experience in Pharmaceutical/CRO- Good knowledge of programming languages (SAS Macros, SQL, STATS, graph and ODS) with an understanding ...
Principal Programmer Analyst role at Thermo Fisher Scientific leading statistical and bioinformatics programming for clinical trials. The position involves project oversight, team leadership, process improvements, and client interactions across multiple drug programs and studies. Responsibilities - Lead programmer or project ...
... cross-functional teams. - Represent programming in internal study meetings and client/sponsor discussions. - Provide technical guidance and mentoring to junior and senior programmers. - Identify opportunities for SDTM standardization, automation, reusable programming, and process improvement. - Support responses to regulatory ...
ICON seeks a Statistical Analyst to support clinical trial activities, including study design input, statistical methods documentation, and SAS-based programming. The role involves collaborating across teams to deliver high-quality statistical analyses and study deliverables. Responsibilities - Support study initiation ...