Senior Associate - RWE Obesity Statistical Programming

Amgen; Hyderabad; On-site; INR 1,200,000 - 1,600,000; Full time

Job summary

A leading biotechnology company is seeking a Senior Statistical Programmer in Hyderabad, India. This role focuses on generating Real-World Evidence (RWE) to support products throughout the drug development lifecycle. The ideal candidate will have strong programming skills in SAS, R, and SQL, with a background in statistical programming and clinical development. Collaboration with global teams is essential. The company offers a dynamic work environment with opportunities for professional growth.

Qualifications

• 4+ years of experience in statistical programming or application programming.
• Experience with real-world evidence generation in clinical settings.
• Proficient in identifying data anomalies and ensuring program accuracy.

Responsibilities

• Write, test and validate software programs to produce analysis datasets.
• Manage all programming activities according to resource and timeline plans.
• Lead development of programming and process improvement initiatives.

Skills

Statistical programming using SAS

Statistical programming using R

SQL

Python

Communication skills

Education

Bachelor's degree in Computer Science or related field

Master's degree in relevant scientific subject

Tools

Databricks

Job description

Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people’s lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world’s leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.

Observational research (OR) is an increasingly important component in drug development and commercialization, because in the current environment, there is increased demand for information from OR studies for regulatory and reimbursement authorities. The Center for Observational Research (CfOR) at Amgen partners with teams to generate real world evidence for multiple stakeholders across the product lifecycle. CfOR contributes evidence regarding the frequency and distribution of disease or the clinical burden of disease, the natural history or clinical course of disease, the design of clinical trials, cost and utilization patterns, and the safety and effectiveness of interventions.

Position Summary

Amgen is seeking a dedicated Senior Statistical Programmer to join our Center for Observational Research (CfOR) organization, based in Hyderabad, India. This crucial role involves generating Real-World Evidence (RWE) to support Amgen products throughout the drug development lifecycle. The successful applicant will collaborate with teams across multiple time zones to fulfill requests, clarify requirements, escalate issues, and deliver high-quality results. The Senior Statistical Programmer will report to a locally based Biostatistical Programming Manager.

Responsibilities

• Write, test and validate software programs in Unix and Databricks to produce analysis datasets and presentation output such as tables and figures, to be included in reports for submission to regulatory agencies, publications and other communications
• Provide technical solutions to programming problems within CfOR
• Lead and develop technical programming and process improvement initiatives within CfOR
• Represent the programming function and participate in multidisciplinary project team meetings
• Manage all programming activities, according to agreed resource and timeline plans
• Ensure all programming activities on the project adhere to departmental standards
• Write and/or review and approve all programming plans
• Write and/or review and approve analysis dataset specifications
• Review and approve key study-related documents produced by other functions, e.g. SAPs, CRF, Data Management Plan, etc.
• Write, test, validate and execute department-, product- and protocol-level macros and utilities
• Lead and/or participate in the development and review of CfOR policies, SOPs and other controlled documents
• Participate in study and systems audits by Clinical Quality Assurance (CQA) and external bodies, and respond to audit questions and findings
• Participate in the recruitment of programming staff
• Actively participate in external professional organizations, conferences and/or meetings
• Provide input to and participate in intra-departmental and CfOR meetings
• Contribute to the continuous improvement of programming, CfOR, and Research and Development (R&D)
• Manage staff performance and oversee staff assignments and utilization

Basic Qualifications

• Bachelor’s degree in Computer Science, Statistics, Mathematics, Life Sciences, Economics or other relevant scientific subject
• At least four (4) years of relevant statistical programming, systems engineering or application programming experience in a clinical development or life sciences setting
• Experience in SQL, and statistical programming using SAS or R

Preferred Qualifications

• Master’s degree in Computer Science, Statistics, Mathematics, Life Sciences, Economics or other relevant scientific subject
• Training or experience using the Observational Medical Outcomes Partnership (OMOP) common data model

Experience

• Real-world evidence (RWE) generation in pharmaceutical or related research industries, or statistical programming for clinical trials
• Strong individual contributor, proficient in developing analysis datasets, identifying data anomalies, and ensuring program accuracy
• Global collaboration on studies to clarify and implement analyses described in Statistical Analysis Plans
• Project fulfillment, statistical programming, issue escalation, results delivery
• Statistical programming: SQL required; SAS or R required; Python preferred
• Motivated to learn how to work with real-world healthcare data (RWD) such as healthcare claims (MarketScan, Optum Clinformatics, Medicare) and EHR databases (Optum EHR PanTher, Flatiron, CPRD, MDV)

Key Competencies

• Hands-on programming role
• Expert statistical programming knowledge using SAS or R
• Required: SAS or R
• Required: SQL
• Preferred: Python
• Excellent verbal and written communication skills in English
• Ability to have efficient exchanges with colleagues across geographical locations
• Agile project management
• Real-world data (RWD) including insurance claims databases, electronic medical records and patient registries; for example, MarketScan, Optum, PharMetrics, Flatiron, Medicare
• OMOP common data model
• Drug development life cycle
• Statistics and basic epidemiology: Incidence and prevalence
• [Required for Regulatory RWE role]: CDISC (SDTM, ADaM)
• Scientific / technical excellence
• Oral and written communication, documentation skills
• Leadership
• Innovation
• Teamwork
• Problem solving
• Attention to detail
• Learning mindset