Biostatistical Programming Senior Associate (Innovation) in Hyderabad, भारत
Amgen
Hyderabad, भारत
Amgen seeks a Biostatistical Programming Senior Associate in Hyderabad to develop programming efficiencies, automation solutions, and innovative tools for statistical programming teams. This role emphasizes building systems and optimizing workflows rather than hands-on clinical data analysis, with focus on leveraging modern technologies including AI and machine learning.
Responsibilities
Analyze and report clinical trial data using SAS, R, or Python; create and validate SDTM and ADaM datasets
Design, build, and maintain programming solutions and tools that improve efficiency and quality across statistical programming teams
Automate repeatable programming tasks and establish standards for modular, reusable code
Collaborate with programming teams to identify process gaps, prototype scalable solutions, and integrate innovations across centers
Develop and deploy AI agents or copilots to optimize programming workflows; create documentation, training materials, and user guides
Requirements
Bachelor's degree or higher in biostatistics, statistics, mathematics, computer science, or related quantitative field
At least 4 years of statistical programming experience in clinical development environment
Proficiency with SAS and/or R or Python for clinical trial data analysis
Working knowledge of CDISC SDTM, ADaM, and Define standards
Familiarity with data quality and compliance check tools
Excellent English communication skills, both written and oral
Ability to work effectively in globally dispersed team environments
Amgen seeks a Biostatistical Programming Senior Associate in Hyderabad to perform statistical programming for clinical trial data analysis and regulatory submissions. The role involves creating and validating datasets, tables, and figures using SAS and R, with responsibility for complex clinical study programming across ...
Amgen seeks a Biostatistical Programming Senior Associate in Hyderabad to perform statistical programming for clinical trials and regulatory submissions. The role involves SAS/R programming, dataset creation and validation, and collaboration with global cross-functional teams supporting integrated clinical development. ...
Amgen seeks a Biostatistical Programming Senior Associate to perform statistical programming for complex clinical trial data analysis and regulatory submissions. The role is based in Hyderabad and supports integrated delivery across regions, with potential focus on Population PK/PD dataset creation. Responsibilities - Perform ...
Amgen seeks a Senior Manager of Biostatistical Programming to lead offshore statistical programming teams in Hyderabad, overseeing end-to-end clinical trial programming activities, regulatory submissions, and global strategy implementation across product areas. Responsibilities - Lead offshore team of Study Lead Programmers ...
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. ...
... pharmaceutical company, we use science and innovation to develop life-changing medicines for people with serious https://jobeax.com/link/QBe1ZamoJXmfvWX4 are seeking an Associate Manager, Statistical Programming - Central Services to join our Statistical Programming team, supporting integrated analysis, regulatory submissions, and clinical ...
Associate Director of Statistical Programming in the Oncology Biometrics department, responsible for leading statistical programming activities across clinical drug development, regulatory submissions, and commercialization efforts. Reports to the Director of Statistical Programming at a hybrid role in Bangalore. 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 ...
... and statistical reporting documentation Requirements - Master's degree in statistics, biostatistics, mathematics, or related field - 6+ years of relevant biostatistical or statistical experience - Advanced SAS programming proficiency (BASE, STAT, MACRO, GRAPH) - Demonstrated expertise in clinical trial design and statistical ...
... deliverables aligned with clinical trial standards. Responsibilities - Author analysis plans, statistical specifications, and quality control reviews of SAPs and programming shells. - Program datasets, tables, listings, and figures to industry standards while ensuring accuracy and consistency. - Lead biostatistical teams on individual ...