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Meddra Coding Jobs in Raleigh, NC (NOW HIRING)

Senior Medical Coder

Raleigh, NC · On-site +1

$16 - $21.50/hr

Perform dictionary coding in accordance with study specific coding conventions using MedDRA and WHO Drug within various coding systems. Manage end-to-end delivery of clinical data management coding ...

Evaluation of individual case reports considering medical/pharmacological aspects as well as verification of MedDRA/IMDRF coding for adverse events (clinical signs), problem codes impact on health ...

Meddra Coding information

See Raleigh, NC salary details

$8

$18

$28

How much do meddra coding jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for meddra coding in Raleigh, NC is $18.71, according to ZipRecruiter salary data. Most workers in this role earn between $10.96 and $25.91 per hour, depending on experience, location, and employer.

What is a MedDRA Coding job?

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.

What are the key skills and qualifications needed to thrive in the Meddra Coding position, and why are they important?

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.

What are the typical responsibilities of a MedDRA Coding specialist on a clinical research or pharmacovigilance team?

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.

What are the most commonly searched types of Meddra Coding jobs in Raleigh, NC? The most popular types of Meddra Coding jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Meddra Coding jobs? Cities near Raleigh, NC with the most Meddra Coding job openings:
Infographic showing various Meddra Coding job openings in Raleigh, NC as of May 2026, with employment types broken down into 50% Part Time, and 50% Contract. Highlights an 50% In-person, and 50% Remote job distribution, with an average salary of $38,915 per year, or $18.7 per hour.

Senior Medical Coder

Biodata Partners, Inc.

Raleigh, NC • On-site, Remote

$16 - $21.50/hr

Part-time

Posted 10 days ago


Job description

Job Summary:
Perform dictionary coding in accordance with study specific coding conventions using MedDRA and WHO Drug within various coding systems. Manage end-to-end delivery of clinical data management coding responsibilities concurrently for single/multiple projects ensuring quality and timeliness. Provide leadership and mentorship to Medical Coding Specialists as needed. Create, review, and maintain guidance and training documentation for coding guidelines an accordance with ICH guidance, official coding guidelines and dictionary definitions
Responsibilities:
  • Perform coding in accordance with study specific coding conventions as outlined in the Data Management Plan (DMP)
  • Perform coding using MedDRA and WHO Drug of (eCRF) verbatim terms using various coding systems
  • Provide independent review of coded data by ensuring consistent code assignment within a project by reviewing coding and re-assignment
  • Responsible for medical coding review, synonym dictionaries review, therapeutically aligned coding conventions
  • Create, review, and maintain guidance and training documentation for coding guidelines an accordance with ICH guidance, official coding guidelines and dictionary definitions
  • Provide support to other departments concerning dictionary use and code assignment
  • Ensure compliance with industry quality standards, regulations, guidelines and procedures
  • Management of query assignment within eCRF systems for questionable verbatim terms
  • Preparation of specific study coding reports for accuracy and consistency as well as client requirements
  • Interaction with clients regarding specific coding requests and coding timelines
  • Participate in system upgrades, including User Acceptance Testing (UAT) to maintain a validated coding environment
  • Perform coding related study close activities ensuring all coding is accurate and proper documentation is complete
  • Liaise with Clinical Data Managers and Programmers for purposes of project requirements
  • Communicate issues that require decisions, including proposal for a solution
  • CTCAE coding and review

Experience:
  • 5+ years in Pharmaceutical/Biotechnology industry or CRO environment
  • Thorough knowledge and experience with WHODrug AND MedDRA dictionaries
  • Knowledge of ICH/GCP guidelines, 21 CFR Part 11 and clinical trial methodology
  • Excellent verbal and written communication skills
  • Detail oriented, ability to multitask with strong prioritization, planning and organization skills
  • Excellent team player
  • Proficiency in Microsoft Office Applications
  • Working knowledge of MedDRA and WHODrug best practice documents
  • Good understanding of Clinical Data Management processes and the applicable regulatory requirements
  • Good overview of all systems lined to the coding process, and understanding of their interactions and dependencies

Education:
  • Bachelor of Science degree in biology or health-related field preferred

Language Skills Required:
Speaking: English (Required)
Writing/Reading: English (Required)