Senior RWERWA Programmer
New Brunswick, NJ - USA
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 objectivesExpert 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
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