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Senior RWERWA Programmer

Parexel


Job Location:

New Brunswick, NJ - USA

Monthly Salary: Not provided by the employer
Posted: 27 June 2026 (30+ days ago)
Application Deadline: 20 October 2026
Vacancies: 1 Vacancy

Job Summary

When our values align theres no limit to what we can achieve.

At Parexel we all share the same goal - to improve the worlds 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 were committed to making a difference.

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

Join a high-impact team as aremote Sr. Real-World Evidence Analyst Programmer
supporting innovative work acrossCanada 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

  • Expert Coder: The ideal candidate spends most of their time hands-on coding versus project management or oversight responsibilities has hands-on experience with raw RWE data including both claims data and Flatiron EHR and can write SQL code from scratch.

  • Advanced SQL Programming experience within the Real-World Data (RWD) domain is required.

  • Hands-on experience developing and managing data solutions in the Snowflake platform required.

  • Clean andvalidateReal-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 epidemiologicalmethodologyimplementation
    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 meetingobjectivesof the project.

  • Daily work % estimates: Coding (80%-90% of their daily work) copying and pasting the numbers into the excel table shells (5%-20%)

  • 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 knowledgeregardingprogram 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 2-3 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

  • Hands-on experience with Flatiron datarequired; experience with Optum may be considered

  • Fluency in SQL and R programming is

  • Experience writing original codeand 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 communicationand 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.


Required Experience:

Senior IC


About Company

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Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our the ... View more

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