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Associate - Rwe Regulatory Statistical Programming

Amgen
Amgen
2+ years
Not Disclosed
Hyderabad, India
10 March 5, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate – RWE Regulatory Statistical Programming

Location: Hyderabad, India
Company: Amgen
Job Type: Full-Time
Job ID: R-237847
Work Location Type: On Site
Date Posted: March 02, 2026
Experience Required: Minimum 2+ Years

Job Overview
Amgen is seeking a talented Associate – RWE Regulatory Statistical Programming to join the Center for Observational Research (CfOR) in Hyderabad, India. This role supports statistical programming activities that contribute to the generation of Real-World Evidence (RWE) and regulatory submission studies across the drug development lifecycle.

The Associate Biostatistical Programmer will work with multidisciplinary teams to analyze real-world healthcare data and produce statistical outputs required for regulatory submissions, publications, and internal scientific communications. The position requires strong programming expertise, data management skills, and the ability to collaborate with global teams while maintaining compliance with regulatory and company standards.

Key Responsibilities
Develop, test, and validate statistical programs using SAS, SQL, Databricks, or R to generate analysis datasets and presentation outputs such as tables, listings, and figures.

Support statistical analyses for regulatory submission studies and research projects.

Ensure accuracy, completeness, and quality of biomedical data used in regulatory documentation and scientific reports.

Work with large real-world healthcare datasets to support evidence generation and regulatory requirements.

Prepare and maintain programming plans, analysis dataset specifications, and related technical documentation.

Contribute to study-related documents such as Statistical Analysis Plans (SAPs) and Data Management Plans.

Develop and maintain department-, product-, and protocol-level macros and utilities to improve programming efficiency and standardization.

Collaborate with cross-functional teams including epidemiologists, statisticians, and clinical researchers to clarify analytical requirements.

Execute programming tasks according to established timelines, resource plans, and departmental standards.

Participate in project meetings and provide technical programming support for research initiatives.

Ensure all programming activities comply with Amgen policies, SOPs, and regulatory guidelines.

Participate in Clinical Quality Assurance (CQA) audits and external regulatory audits when required.

Contribute to programming process improvements and technical initiatives within the CfOR organization.

Required Qualifications
Bachelor’s degree in Computer Science, Statistics, Mathematics, Life Sciences, Economics, or another relevant scientific discipline.

Experience Required
Minimum 2 years of relevant experience in statistical programming, systems engineering, or application programming within a pharmaceutical, biotechnology, clinical research, or life sciences environment.

Preferred Qualifications
Master’s degree in Computer Science, Statistics, Mathematics, Life Sciences, Economics, or a related field.

Experience working with Real-World Evidence (RWE) research or clinical research datasets.

Familiarity with modern data processing platforms and programming environments.

Technical Skills
Proficiency in statistical programming using SAS or R.

Strong knowledge of SQL for data extraction and analysis.

Understanding of CDISC standards such as SDTM and ADaM.

Experience working with real-world healthcare data including claims databases, electronic health records, and patient registries.

Exposure to programming environments such as Databricks or Unix systems is an advantage.

Key Competencies
Strong analytical and problem-solving abilities.

Attention to detail and commitment to data accuracy.

Excellent written and verbal communication skills.

Ability to collaborate effectively with global cross-functional teams.

Strong documentation and reporting skills.

Teamwork, adaptability, and continuous learning mindset.

About Amgen
Amgen is a global biotechnology company focused on discovering, developing, manufacturing, and delivering innovative human therapeutics for patients suffering from serious illnesses. Since its founding in 1980, Amgen has grown into one of the world’s leading biotechnology organizations, serving millions of patients globally.

Through its Center for Observational Research (CfOR), Amgen generates real-world evidence that supports clinical development, regulatory decision-making, and healthcare policy. By combining scientific innovation, advanced analytics, and global collaboration, Amgen continues to develop breakthrough therapies that address areas of high unmet medical need and improve health outcomes worldwide.