Associate Director, Real World Evidence Data Scientist job opportunity at AstraZeneca.

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AstraZeneca Associate Director, Real World Evidence Data Scientist
Experience: 3-years
Pattern: full-time
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Real World Evidence Data Scientist

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degreeAssociate
loacation US - Gaithersburg - MD, United States Of America
loacation US - Gaithersb..........United States Of America

Associate Director, Real World Evidence Data Scientist Introduction to the role The Centre for Oncology Data Excellence (CODE) is a function that is focused on delivering best in class scientifically rigorous research to support Global Medical Evidence Generation. Within CODE, the Real World Evidence (RWE) Data Scientist will be part of the Oncology Data & Analytics (ODA) team, responsible for real-world data (RWD) analysis, Data Foundation & Governance, Analytics Platforms/Tools and innovative AI capabilities. As a member within the ODA team, your collaboration will span multiple functions within Medical Evidence Generation. The ideal candidate for this role will bring a proven track record of delivering value through the utilization of routinely collected data from healthcare settings, providing health analytics and insights in various contexts including Public Health, Pharmaceutical Research and Development, and Commercial/Payer sectors. They will collaborate with colleagues in Oncology Outcomes Research (O2R), Epidemiology, and Statistics to provide scientific and technical guidance on study design, data selection, best practices in using RWD, and implementing advanced statistical methods. With the rapid development of GenAI, the successful candidate will be expected to leverage cutting-edge AI tools to scale analytics tasks and augment data insights. Accountabilities: Collaborate with key stakeholders, including outcomes research and next-gen science groups to support study design, conduct RWD feasibility assessments, and execute protocol-driven and insight projects to a high standard. Maintain in-depth knowledge of real-world oncology data sources (claims, EHR, and registries). Provide strong insights into the strengths and limitations of in-house data sources to facilitate data suitability assessments for study planning. Translate ambiguous business and scientific questions into clear, actionable analytic specifications and programming tasks (R/Python/SQL). Champion reusable code libraries, version control, and reproducible data science workflows. Stay current with methodological developments in real world evidence (RWE) generation, including causal inference, ECA, ML/AI methods, and federated learning/OMOP, and provide clear technical input on study design and analysis. Incorporate LLMs/GenAI, agentic workflows and AI coding tools into day-to-day workflows to accelerate code development, discovery, documentation, review, and insight generation. Communicate complex methods and analysis results clearly to both technical and non-technical audiences internally and externally. Essential Skills/Experience: PhD or MS in epidemiology, biostatistics, data science, computer science, or related field such as health informatics with at least 3 years of relevant pharmaceutical industry or CRO experience. Experience in RWE and familiarity with observational study methodologies. At least 5+ years of experience working directly with large, complex healthcare datasets (claims/EHR/registries) in quantitative research. Demonstrated proficiency in R/Python and SQL. Expertise in developing FAIR-compliant data analytics pipelines supported by use of version control tools like GitHub and agile tools like JIRA. Proven ability to build long-term and trusted partnerships with cross-functional stakeholders, manage conflicts and competing priorities to drive timely, high-quality outcomes. Strong and effective communication skills, both oral and written. Demonstrated ability to articulate research questions and translate them into structured data analysis plans and technical workstreams that deliver measurable business value. Proficiency in applying GenAI-based coding assistants (e.g., GitHub Copilot) and agentic tools to support project planning, data analysis, code review, or scientific documentation workflows. A curious learner who continuously deepens disease knowledge, RWD expertise and explores emerging technologies and RWE methodologies to meet evolving stakeholder needs. Desirable Skills/Experience: Expertise in clinical data standards, medical terminologies, and controlled vocabularies used in healthcare data and ontologies (e.g., ICD-9/10, NDC, HCPCS). Ability to lead and manage cross-functional data science projects with track record of peer-reviewed publications and/or regulatory submissions. Demonstrated experience with building production grade analytics solutions using tools such as R (Shiny) or Python (Dash). Excellent organizational and project management skills with demonstrated ability to prioritize and manage multiple tasks. Experience with AI-empowered software and web application development in pharmaceutical, biomedical, or healthcare sectors. The annual base pay for this position ranges from $ 135,457.60 - 203,186.40 USD . Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program. Benefits offered include a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. Why AstraZeneca? 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. At AstraZeneca, we are proud to work on the cutting-edge with one of the broadest and deepest Oncology pipelines in the business. Our Medical Affairs team is dedicated to changing the practice of medicine by generating compelling medical evidence that improves patient experiences. We foster a culture of openness and transparency, empowering our team members to take a tailored approach to their development. By collaborating with experts across the industry, we create innovative scientific evidence that transforms how patients living with cancer are treated. Join us in our mission to redefine cancer treatment! Ready to make an impact? Apply now and be part of our journey to eliminate cancer as a cause of death! Date Posted 22-Jan-2026 Closing Date 04-Feb-2026 Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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