Senior RWE​/RWA Programmer

Parexel is seeking a Senior Real-World Evidence (RWE) Analyst Programmer

Join a high-impact team as a remote Sr. Real-World Evidence Analyst Programmer, supporting innovative work across Canada or the Continental United States.

If you are passionate about real-world data, advanced analytics, and delivering meaningful insights, we encourage you to apply.

• Effectively designs and codes R and SQL programs for assigned project(s), consistently meeting project objectives.
• Clean and validate Real-World Data (RWD) to ensure consistency and reliability.
• Implement programming based on RWE protocols using a variety of RWD sources, including Optum and Flatiron.
• Leverage advanced statistical and epidemiological methodologies to deliver robust and reliable analyses.
• Create, review, and approve programming plans at both study and project levels.
• Demonstrate advanced knowledge of programming, epidemiological methodology implementation, and system development life cycle concepts.
• Maintain clear documentation of analytical programming and operational definitions to support reproducible and auditable RWE studies.
• Develop dashboards, reports, and presentations to effectively communicate findings.
• Collaborate with study team members to meet study timelines and recurring reporting deadlines.

• Effectively design and code R and SQL programs for assigned project(s) consistently meeting objectives of the project.
• Clean and validate RWD for consistency and reliability.
• Implement programming as specified from RWE protocol using a variety of RWD from multiple sources, including Optum and Flatiron.
• Leverage advanced statistical and epidemiological methodologies to deliver robust and reliable analyses.
• Create or review and approve programming plans at study and project level.
• Displays highly advanced knowledge regarding programming, epidemiology methodologies implementation and system development life cycle concepts.
• Maintain clear documentation of analytical programming and operational definitions to support reproducible and auditable RWE studies.
• Develop dashboards, reports, and presentations to communicate findings.
• Work collaboratively with members of study teams to meet study and recurring report timelines.

• MS in data science, epidemiology, statistics, public health, or related discipline.
• At least 7 years of experience in Real-World Data (RWD) analysis and Real-World Analytics (RWA) using healthcare claims, EMR, and/or registry databases within the biopharmaceutical industry or provider/payer organizations.
• Includes strong hands‑on experience with Optum and/or Flatiron data.
• Fluency in SQL and R programming is required.
• Experience writing original code and performing raw data analysis (not derived solely from clinical trials).
• Includes running analyses and/or developing code for real‑world analyses.
• Knowledge of SAS and/or Python is considered an advantage.
• Familiarity with US and global healthcare coding systems (e.g., ICD, CPT, HCPCS, LOINC, MedDRA).
• And healthcare delivery systems (e.g., payers and reimbursement models).
• Experience conducting routine and advanced statistical analyses for RWE generation
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• Including time‑to‑event, cross‑sectional, and longitudinal data.
• Experience with big data analytical platforms
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• Deep understanding of observational study analysis
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• Ability to work independently and contribute to scrum development goals
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• In a fast‑paced, flexible, team‑oriented environment.
• Strong communication and collaboration skills.
• Competent in written and oral English.

Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.