AstraZeneca Posted August 10, 2026

Associate Director I/II, Real World Data Statistics

Bangalore, India Full time
Biostatistics & Data Science Associate Director

AstraZeneca is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Job Title: Associate Director I/II, Real World Data Statistics

Global Career Level: E

Role: Individual contributor role

Location: Manyata Tech Park, Bangalore.

About Alexion

At Alexion, our mission is to transform the lives of people affected by rare diseases through the development and delivery of innovative medicines as well as supportive technologies and healthcare services.

Introduction to role:

Do you thrive at the intersection of statistics, real-world evidence, and regulatory science? Step into a role where your expertise in disease registries and longitudinal observational cohorts directly advances therapies for patients. You will lead the development of regulatory-grade evidence from real-world data, guiding submissions that can speed approvals, support label expansions, and fulfill post-market commitments.

Can you envision turning registry data into decisive insights that withstand health authority scrutiny? Joining our growing epidemiology and real-world evidence capability, you will apply statistical methodologies tailored for registries, align to AstraZeneca standards, and contribute to a portfolio that demands rigor, creativity, and impact.

Accountabilities:

Registry Evidence Strategy: Oversee the statistical vision and analytical strategies for registry-based evidence, crafting regulatory submissions and decisions across rare disease programs.

Regulatory-Grade Analyses: Oversee the design, implementation, and validation of survival, causal inference, propensity score, and longitudinal models tailored for registry data; produce analyses that meet global regulatory expectations.

Methodological Innovation: Define, program, and implement robust, registry-specific statistical approaches addressing challenges such as missingness, data linkage, confounding, and outcome validation; elevate practice through shared findings.

Cross-Functional and External Collaboration: Provide leadership to clinical, epidemiology, regulatory, and registry operations teams; represent Alexion in external forums, advisory boards, and regulatory discussions.

Standards, Quality, and Compliance: Lead and ensure alignment with AstraZeneca standard methodologies and guidance (e.g., FDA RWE Framework, EMA registry guidance); ensure reproducibility, audit readiness, and transparent reporting in statistical deliverables.

Communication and Influence: Translate analytical results into narratives for executive leadership, briefing documents, and regulatory submissions, creating influence at the program level.

People Leadership and Capability Building: Serve as a mentor and coach to other Real World Data Statisticians within the team; build capability through knowledge-sharing, code review, and career development guidance.

Essential Responsibilities:

Lead and oversee the design and implementation of advanced statistical analyses of data from disease registries, patient registries, natural history studies, EMR, and claims data for regulatory submissions, including survival analysis, inference methods, propensity score matching, longitudinal modeling, and registry-specific statistical approaches that align with regulatory guidelines

Drive cross-functional collaboration, partnering with registry teams in regulatory interactions and advisory meetings, ensuring registry-derived analyses align with regulatory strategy and meet health authority expectations for FDA, EMA, and other global regulatory submissions

Oversee the development of regulatory-quality deliverables including statistical analysis plans, tables/figures/listings, and regulatory briefing documents based on registry analyses, ensuring compliance with FDA Real-World Evidence Framework, EMA guidance on registry-based studies, and regulatory guidance documents

Oversee the development and validation of statistical methodologies for real-world evidence generation from registry sources that meet regulatory standards, while leading the engagements with external registry investigators, statisticians, and regulatory consultants to ensure methodological rigor and alignment with regulatory requirements

Mentor, guide, and support the professional development of other Real World Data Statisticians within the epidemiology team, building a high-performing, technically excellent function.

Desirable Skills/Experience:

PhD degree with minimum 7 years of relevant industry experience, or Master’s degree with minimum 10 years of relevant industry experience .

Advanced degree or equivalent experience in statistics, biostatistics, epidemiology.

Expert proficiency with R and/or SAS for analytics; solid understanding of SQL or Python for data engineering and validation

Proven track record of generating real-world evidence for rare disease programs or patient populations

Demonstrated ability of leading regulatory submissions using registry-based analyses and presenting in health authority or advisory settings

Leadership in peer-reviewed publications or conference presentations in pharmacoepidemiology, methodology, or applied real-world evidence

Extensive expertise in data quality assessment, cohort construction, linkage, and missing data strategies for registries

Outstanding communication and influencing skills with the ability to translate sophisticated concepts into clear recommendations for senior leadership

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

AstraZeneca provides the chance to work at the forefront of rare disease biopharma. Here, complex biology and advanced technology come together to compose transformative medicines for individuals with devastating conditions. At Alexion within AstraZeneca Rare Disease, work is driven by a deep connection to patients’ lived experiences and a clear purpose that shapes decisions every day. The environment combines the agility of a biotech with the reach and resources of a global organization, encouraging curiosity, transparent science, ethical decision-making, and continuous learning. Teams collaborate across disciplines to explore rare opportunities in areas of high unmet need while investing in personal growth through tailored development programs that build both technical mastery and empathy for patients’ journeys.

Call to Action:

Ready to turn registries into regulatory-grade evidence that advances therapies for people with rare diseases, share your CV and start crafting what comes next!

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status.

Date Posted

10-Aug-2026

Closing Date

16-Aug-2026

Alexion is proud to be an Equal Employment Opportunity and Affirmative Action employer. We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness. The Company will not make decisions about employment, training, compensation, promotion, and other terms and conditions of employment based on race, color, religion, creed or lack thereof, sex, sexual orientation, age, ancestry, national origin, ethnicity, citizenship status, marital status, pregnancy, (including childbirth, breastfeeding, or related medical conditions), parental status (including adoption or surrogacy), military status, protected veteran status, disability, medical condition, gender identity or expression, genetic information, mental illness or other characteristics protected by law. Alexion provides reasonable accommodations to meet the needs of candidates and employees. To begin an interactive dialogue with Alexion regarding an accommodation, please contact accommodations@Alexion.com . Alexion participates in E-Verify.

Job details

Seniority
Associate Director
Function
Biostatistics & Data Science
Therapeutic area
Not listed
Location
Bangalore, India
Employment type
Full time

How this role compares

Computed from every other active Biostatistics & Data Science role in our database, not just this employer's listings.

We currently track 61 comparable Associate Director Biostatistics & Data Science roles across 17 biopharma companies.

61Comparable roles tracked
51Currently active
17Companies hiring similar roles
12Countries represented

Salary context

22 of 61 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Sr. Computational Statistician (R2 – R3) · Lilly $46,842/yr – $117,289/yr
Highest disclosed · Associate Director, Functional Genomics, Data Science · Merck $176,200/yr – $277,300/yr
Peer group range $82,066 – $226,750 (median $159,000)

Where these roles are based

Top locations among the 61 comparable roles

United States33
India6
Poland5
United Kingdom5
Canada2
Spain2

+ 6 more countries

Seniority mix

61 of 61 peers have a known seniority level

Senior27
Manager24
Associate Director10

Therapeutic area mix

9 of 61 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology9

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

50%similar
Bristol-Myers Squibb Business Services India Private Limited Hyderabad, India Manager
Same function Adjacent seniority Same country
50%similar
Amgen Technology Pvt Ltd. Hyderabad, India Manager
Same function Adjacent seniority Same country
50%similar
Novo Nordisk Bangalore, India Senior
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50%similar
Novo Nordisk Bangalore, India Senior
Same function Adjacent seniority Same country
50%similar
AstraZeneca Bangalore, India Senior
Same function Adjacent seniority Same country
50%similar
Bristol-Myers Squibb Business Services India Private Limited Hyderabad, India Manager
Same function Adjacent seniority Same country

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

50%
Senior Manager, Data Science
Bristol-Myers Squibb Business Services India Private Limited · Hyderabad, India · Manager
Function Therapeutic area Adjacent seniority Country
50%
Associate Senior Clinical Data Scientist (Bangalore, Karnataka, IN)
Novo Nordisk · Bangalore, India · Senior
Function Therapeutic area Adjacent seniority Country
45%
Assoc Director, Statistical Programming
Novartis · East Hanover, United States · Associate Director
Function Therapeutic area Seniority Country
45%
Associate Director, Biostatistics
RayzeBio, Inc · Remote, United States · Associate Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.