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Director, Real World Data Science

6-10 years
Not Disclosed
10 Nov. 27, 2025
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

Director, Real World Data Science (Real World Statistics)

Location: Bengaluru, Karnataka, India
Job ID: R-235769
Posted On: 02 November 2025
Experience Required: 6–12 years in Real World Evidence, Biostatistics, Epidemiology, or regulatory-focused data science


About the Role

AstraZeneca’s Rare Disease Unit (Alexion) is seeking a highly skilled Director, Real World Data Science to lead statistical strategy and analysis for real-world evidence (RWE) initiatives supporting rare disease programs. This role sits within the Epidemiology and Real World Science team and focuses on designing, executing, and interpreting statistical analyses for disease registries, natural history studies, EMR datasets, and claims data to support global regulatory submissions.

With AstraZeneca’s strong legacy in Real World Evidence and regulatory application of registry data, this position offers the opportunity to shape analytical frameworks, guide high-impact regulatory interactions, and mentor emerging statistical talent.


Key Responsibilities

  • Lead the design and implementation of advanced statistical analyses using real-world data sources including patient registries, disease registries, natural history studies, EMR, and claims datasets.

  • Support regulatory submissions by developing statistical strategies aligned with regulatory expectations.

  • Collaborate closely with registry teams to ensure alignment with overall regulatory and clinical development objectives.

  • Generate high-quality statistical outputs including reports, clinical study reports, and regulatory submission documentation.

  • Develop, validate, and implement statistical methodologies tailored to real-world data and registry-based evidence generation.

  • Mentor junior statisticians and data scientists in regulatory-compliant analysis practices.

  • Provide expert guidance on statistical standards, RWE frameworks, and methodologies across cross-functional teams.


Essential Skills & Experience

  • PhD in Biostatistics, Statistics, Epidemiology, Mathematics, Data Science, or related field with a minimum of 6 years’ industry experience, preferably in pharmaceuticals, biotechnology, or consulting.
    OR

  • Master’s degree in a quantitative field with at least 10 years of relevant industry experience.

  • Strong expertise in statistical programming using R, SAS, SQL and regulatory-aligned programming standards.

  • Experience designing analyses for real-world data sources, especially registries and longitudinal observational cohorts.

  • Ability to work effectively in an office environment with proficiency in digital communication, analytical problem-solving, and cross-functional collaboration.


Desirable Skills & Experience

  • Proven success in regulatory submissions involving registry-derived evidence.

  • Deep understanding of global regulatory guidance, including ICH standards, FDA RWE Framework, EMA registry-based study guidance.

  • Strong background in regulatory statistics with direct experience leading registry-focused analytical programs.

  • Capability to build long-term professional relationships with regulatory authorities.

  • Leadership experience managing multidisciplinary statistical or RWE projects.


Work Model

AstraZeneca encourages in-person collaboration, with an expectation of working a minimum of three days per week from the office while supporting flexibility based on individual needs.


Why Join AstraZeneca | Alexion Rare Disease

At AstraZeneca, you will be part of a culture rooted in innovation, inclusivity, scientific excellence, and patient commitment. You will collaborate with experts across functions, contribute to meaningful healthcare advancements, and access structured career development pathways. This is an opportunity to influence regulatory science and real-world methodology for rare diseases at a global level.