Senior RWE/RWA Programmer

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 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

• 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.

• 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 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 isrequired

• 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.