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Senior RWE/RWA Programmer
Parexel · United States - Remote; 14 Locations; Canada-Quebec-Remote; Canada-Prince Edward Island-Remote; Canada-New Brunswick-Remote; Canada-Northwest Territories-Remote; Canada-Newfoundland and Labrador-Remote; Canada-Manitoba-Remote; Canada-Nunavut-Remote; Canada-Yukon-Remote; Canada-Alberta-Remote; Canada-Ontario-Remote; Canada-Nova Scotia-Remote; Canada-Saskatchewan-Remote; Canada-British Columbia-Remote · Remote · Active · Workday Recruiting
Job facts
| Field | Value |
|---|---|
| Company | Parexel |
| Title | Senior RWE/RWA Programmer |
| Normalized title | - |
| Department / team | - |
| Location | United States |
| Work model | Remote / Remote |
| Employment type | - |
| Salary | - |
| Status | active |
| ATS provider | Workday Recruiting |
| Posted / first seen | 2026-06-18 / 2026-06-19 |
| Changed / last seen | 2026-06-20 / 2026-06-20 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Parexel. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through Workday Recruiting. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| Work model jobs | Active Remote postings. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Parexel |
| Source | a38f5933-8d87-4b90-bb56-84b4c1881427 |
| ATS provider | Workday Recruiting |
Description
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
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.
Who We Are Looking For
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
What You Will Do
Effectively designs and codes 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 program, 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
Who You Are
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
Including time-to-event, cross-sectional, and longitudinal data
Experience with big data analytical platforms
Deep understanding of observational study analysis
Ability to work independently and contribute to scrum development goals
In a fast-paced, flexible, team-oriented environment
Strong communication and collaboration skills
Competent in written and oral English.
EEO Disclaimer
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.
Full job record
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| Provider | workday |
| Provider Job Key | /job/United-States---Remote/Senior-RWE-RWA-Programmer_R0000042912 |
| Title | Senior RWE/RWA Programmer |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | United States - Remote; 14 Locations; Canada-Quebec-Remote; Canada-Prince Edward Island-Remote; Canada-New Brunswick-Remote; Canada-Northwest Territories-Remote; Canada-Newfoundland and Labrador-Remote; Canada-Manitoba-Remote; Canada-Nunavut-Remote; Canada-Yukon-Remote; Canada-Alberta-Remote; Canada-Ontario-Remote; Canada-Nova Scotia-Remote; Canada-Saskatchewan-Remote; Canada-British Columbia-Remote |
| Department | — |
| Team | — |
| Employment Type | — |
| Workplace Type | remote |
| Remote Policy | remote |
| Country | United States |
| Region | — |
| City | — |
| Salary Raw | — |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://wd1.myworkdaysite.com/recruiting/parexel/Parexel_External_Careers/job/United-States---Remote/Senior-RWE-RWA-Programmer_R0000042912 |
| Apply URL | https://wd1.myworkdaysite.com/recruiting/parexel/Parexel_External_Careers/job/United-States---Remote/Senior-RWE-RWA-Programmer_R0000042912 |
| First Seen At | 2026-06-19 09:38:01Z |
| Last Seen At | 2026-06-20 08:53:10Z |
| Last Checked At | 2026-06-20 08:53:10Z |
| Last Changed At | 2026-06-20 08:53:10Z |
| Inactive At | — |
| Source Posted At | 2026-06-18 00:00:00Z |
| Source Updated At | — |
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"jobDescription": "<p><b>When our values align, there's no limit to what we can achieve.</b><br /> <br />At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.</p><p></p><p>Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.</p><p></p><p></p><div><p><span> </span></p></div><div><p><b><span>Parexel is seeking a Senior Real-World Evidence (RWE) Analyst Programmer</span></b><span> </span></p></div><div><p><span><span>Join a high-impact team as a<span> </span></span></span><b><span>remote Sr. Real-World Evidence Analyst Programmer</span></b><span><span>,</span></span><span><span> </span></span><br /><span><span>supporting innovative work across<span> </span></span></span><b><span>Canada or the Continental United States</span></b><span><span>.</span></span><span> </span></p></div><div><p><span><span>If you are passionate about real-world data, advanced analytics,</span></span><span><span> </span></span><br /><span><span>and delivering meaningful insights, we encourage you to apply.</span></span><span> </span></p></div><div><p><b><span>Who We Are Looking For</span></b><span> </span></p></div><div><ul><li><p><b><span>Effectively designs and codes R and SQL programs</span></b><span><span> </span></span><br /><span><span>for assigned project(s), consistently meeting project objectives</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Clean and<span> </span></span><span>validate</span><span><span> </span>Real-World Data (RWD)</span></b><span><span> </span></span><br /><span><span>to ensure consistency and reliability</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Implement programming based on RWE protocols</span></b><span><span> </span></span><br /><span><span>using a variety of RWD sources, including Optum and Flatiron</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Leverage advanced statistical and epidemiological methodologies</span></b><span><span> </span></span><br /><span><span>to deliver robust and reliable analyses</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Create, review, and approve programming plans</span></b><span><span> </span></span><br /><span><span>at both study and project levels</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Demonstrate advanced knowledge</span></b><span><span> </span></span><br /><span><span>of programming, epidemiological<span> </span></span><span>methodology</span><span><span> </span>implementation,</span></span><span><span> </span></span><br /><span><span>and system development life cycle concepts</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Maintain clear documentation</span></b><span><span> </span></span><br /><span><span>of analytical programming and operational definitions</span></span><span><span> </span></span><br /><span><span>to support reproducible and auditable RWE studies</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Develop dashboards, reports, and presentations</span></b><span><span> </span></span><br /><span><span>to effectively communicate findings</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Collaborate with study team members</span></b><span><span> </span></span><br /><span><span>to meet study timelines and recurring reporting deadlines</span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div><div><p><b><span>What You Will Do</span></b><span> </span></p></div><div><ul><li><p><b><span>Effectively designs and codes R and SQL programs for assigned project(s)</span></b><span><span> </span></span><br /><span><span>consistently meeting<span> </span></span><span>objectives</span><span><span> </span>of the project.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Clean and validate RWD</span></b><span><span> </span></span><br /><span><span>for consistency and reliability</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Implement programming as specified from RWE protocol</span></b><span><span> </span></span><br /><span><span>using a variety of RWD from multiple sources, including Optum and Flatiron</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Leverage advanced statistical and epidemiological methodologies</span></b><span><span> </span></span><br /><span><span>to deliver robust and reliable analyses</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Create or review and approve programming plans</span></b><span><span> </span></span><br /><span><span>at study and project level.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Displays highly advanced knowledge<span> </span></span><span>regarding</span><span><span> </span>program, epidemiology methodologies implementation</span></b><span><span> </span></span><br /><span><span>and system development life cycle concepts.</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Maintain clear documentation of analytical programming and operational definitions</span></b><span><span> </span></span><br /><span><span>to support reproducible and auditable RWE studies</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Develop dashboards, reports, and presentations</span></b><span><span> </span></span><br /><span><span>to communicate findings</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Work collaboratively with members of study teams</span></b><span><span> </span></span><br /><span><span>to meet study and recurring report timelines</span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div><div><p><b><span>Who You Are</span></b><span> </span></p></div><div><ul><li><p><b><span>MS in data science, epidemiology, statistics, public health, or related discipline</span></b><span> </span></p></li></ul></div><div><ul><li><p><b><span>At least 7 years of experience in Real-World Data (RWD) analysis and Real-World Analytics (RWA)</span></b><span><span><span> </span>using healthcare claims, EMR, and/or registry databases within the biopharmaceutical industry or provider/payer organizations</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Includes strong hands-on experience with Optum and/or Flatiron data</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Fluency in SQL and R programming is<span> </span></span><span>required</span></b><span> </span></p></li></ul></div><div><ul><li><p><b><span>Experience writing original code</span></b><span><span><span> </span>and performing raw data analysis (not derived solely from clinical trials)</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Includes running analyses and/or developing code for real-world analyses</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Knowledge of SAS and/or Python is considered an advantage</span></b><span> </span></p></li></ul></div><div><ul><li><p><b><span>Familiarity with US and global healthcare coding systems</span></b><span><span> </span></span><br /><span><span>(e.g., ICD, CPT, HCPCS, LOINC, MedDRA)</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>And healthcare delivery systems (e.g., payers and reimbursement models)</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Experience conducting routine and advanced statistical analyses for RWE generation</span></b><span> </span></p></li></ul></div><div><ul><li><p><span><span>Including time-to-event, cross-sectional, and longitudinal data</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Experience with big data analytical platforms</span></b><span> </span></p></li></ul></div><div><ul><li><p><b><span>Deep understanding of observational study analysis</span></b><span> </span></p></li></ul></div><div><ul><li><p><b><span>Ability to work independently and contribute to scrum development goals</span></b><span> </span></p></li></ul></div><div><ul><li><p><span><span>In a fast-paced, flexible, team-oriented environment</span></span><span> </span></p></li></ul></div><div><ul><li><p><b><span>Strong communication</span><span><span> </span>and collaboration skills</span></b><span> </span></p></li><li><p><b>Competent in written and oral English.</b></p></li></ul></div><p></p><p><b>EEO Disclaimer</b><br />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.</p><p></p>",
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