New Brunswick, NJ · On-site +1
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 ...
New Brunswick, NJ · On-site +1
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 ...
Piscataway, NJ · On-site
$90K - $110K/yr
... code AE's, medical conditions, medications, laboratory results and procedures using MedDra Dictionary. * Collaborate with regulatory and PV Operations departments for AE data gathering, AE ...
Piscataway, NJ · On-site
$90K - $110K/yr
... code AE's, medical conditions, medications, laboratory results and procedures using MedDra Dictionary. * Collaborate with regulatory and PV Operations departments for AE data gathering, AE ...
Piscataway, NJ · On-site
$90K - $110K/yr
... code AE's, medical conditions, medications, laboratory results and procedures using MedDra Dictionary. * Collaborate with regulatory and PV Operations departments for AE data gathering, AE ...
Piscataway, NJ · On-site
$90K - $110K/yr
... code AE's, medical conditions, medications, laboratory results and procedures using MedDra Dictionary. * Collaborate with regulatory and PV Operations departments for AE data gathering, AE ...
Piscataway, NJ · On-site
$90K - $110K/yr
... code AE's, medical conditions, medications, laboratory results and procedures using MedDra Dictionary. * Collaborate with regulatory and PV Operations departments for AE data gathering, AE ...
Piscataway, NJ · On-site
$90K - $110K/yr
... code AE's, medical conditions, medications, laboratory results and procedures using MedDra Dictionary. * Collaborate with regulatory and PV Operations departments for AE data gathering, AE ...
$9.99 - $12.05
21% of jobs
$12.48 is the 25th percentile. Wages below this are outliers.
$12.05 - $14.11
20% of jobs
$14.11 - $16.16
8% of jobs
The median wage is $16.57 / hr.
$16.16 - $18.22
5% of jobs
$18.22 - $20.27
0% of jobs
$20.27 - $22.33
0% of jobs
$22.33 - $24.39
0% of jobs
$24.39 - $26.44
9% of jobs
$28.50 is the 75th percentile. Wages above this are outliers.
$26.44 - $28.50
11% of jobs
$28.50 - $30.55
13% of jobs
$30.55 - $32.61
13% of jobs
$9
$21
$32
A MedDRA Coding job involves assigning standardized Medical Dictionary for Regulatory Activities (MedDRA) terms to adverse events, medical conditions, and drug-related data in clinical trials and pharmacovigilance. Coders ensure consistency and accuracy in medical terminology to support regulatory reporting and safety analysis. This role requires knowledge of MedDRA hierarchy, coding guidelines, and industry regulations. Professionals often work in pharmaceutical companies, contract research organizations (CROs), or regulatory agencies. Strong attention to detail and familiarity with medical terminology are essential skills for this job.
To excel in MedDRA Coding, a strong understanding of medical terminology, clinical research processes, and pharmacovigilance concepts—often supported by a life sciences degree or healthcare background—is essential. Familiarity with the MedDRA (Medical Dictionary for Regulatory Activities) system, coding software, and relevant regulatory guidelines, along with certifications in drug safety or medical coding, is highly valued. Attention to detail, analytical thinking, and effective communication are standout soft skills for this position. These competencies are crucial to ensure accurate and consistent coding of medical terms, enabling high-quality safety data analysis and regulatory compliance.
A MedDRA Coding specialist is primarily responsible for translating medical information from clinical trial reports, adverse event forms, or safety databases into standardized MedDRA terms. This ensures accurate data capture, analysis, and reporting for regulatory submissions and ongoing safety monitoring. Specialists often collaborate with drug safety teams, medical writers, and data managers to resolve coding discrepancies and maintain consistency in terminology. In addition, the role may involve participating in cross-functional meetings and providing coding support during audits or inspections. Working efficiently and maintaining up-to-date knowledge of MedDRA updates are also key aspects of the job.
8.2
Based on 13 frontline employees who took The Breakroom Quiz
29th of 73 rated research
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
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 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.
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Bring your Data Management expertise to Parexel's Strategic Partnerships. Although we work globally, each partnership we form is deeply personal. We are as dedicated to every aspect of our client's product development as they are - and work closely with client teams in true partnership to understand both challenges and opportunities. At Parexel we are focused on meeting customer and patient needs through collaborative partnership so that we get treatments into the hands of patients who need them most.
Pharmaceutical and medicine manufacturing
10,000+ Employees
Waltham, MA, US
1983
