Statistical Programmer

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.

What you will do

Amgen is seeking a dedicated Associate Biostatistical 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 Associate Biostatistical Programmer will report to a locally based Biostatistical Programming Manager.

The Associate Biostatistical Programmer will be responsible for hands-on programming and results delivery. Additionally, they will be responsible for manipulating large databases and generating reports to enable epidemiologists to explore and generate RWE from real-world healthcare data assets. The ideal candidate should possess a bachelor’s degree and have at least two years of relevant career experience in statistical programming. Proficiency in SAS and SQL programming is required, while experience with R and Python is preferred. The successful candidate will demonstrate scientific and technical excellence, exceptional oral and written communication skills, problem-solving abilities, and meticulous attention to detail. The ability to work effectively within a large, globally distributed team is essential.

• 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

• Write, test, validate and execute department-, product- and protocol-level macros and utilities

• Participate in study and systems audits by Clinical Quality Assurance (CQA) and external bodies, and respond to audit questions and findings

• 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)

What we expect of you

• Bachelor’s degree and 0 to 3 years of Computer Science, Information Technology, or a related field OR

• Diploma and 4 to 7 years of Computer Science, Information Technology, or a related field.

Experience:

• 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: SAS and SQL required; R and 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)

Preferred Qualifications:

• Training or experience using the Observational Medical Outcomes Partnership (OMOP) common data model.

Key Competencies

• Hands-on programming role

• Expert statistical programming knowledge using SAS or R

• Required: SAS

• Required: SQL

• Preferred: R

• Preferred: Python

• Excellent verbal and written communication skills in English

• Ability to have efficient exchanges with colleagues across geographical locations

• Real-world data (RWD) including insurance claims databases, electronic medical records and patient registries; for example, MarketScan, Optum, PharMetrics, Flatiron, Medicare

• Scientific / technical excellence

• Oral and written communication, documentation skills

• Leadership

• Innovation

• Teamwork

• Problem solving

• Attention to detail

• Learning mindset

EQUAL OPPORTUNITY STATEMENT

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.