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Meddra Jobs in Raleigh, NC (NOW HIRING)

Biodata Partners, Inc.

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 ...

IQVIA, Inc.

Mgr, Database Management Systems

Durham, NC · On-site

$84K - $211K/yr

Knowledge of MedDRA, WHODrug, annotated CRFs, and data mapping specifications. * Experience with Veeva, Medrio, Oracle Clinical, TrialGrid, or similar EDC systems. * Demonstrated ability to lead ...

GRIFOLS, S.A.

Drug Safety Scientist

Clayton, NC · On-site

Provide Supervision of information entered into the safety database ensuring accuracy, consistency of data, and appropriate MedDRA and WhoDrug coding. * Reviewing worklists on a regular basis to ...

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See Raleigh, NC salary details

$13

$24

$35

How much do meddra jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for meddra in Raleigh, NC is $24.77, according to ZipRecruiter salary data. Most workers in this role earn between $20.10 and $28.27 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a MedDRA Specialist, and why are they important?

To thrive as a MedDRA Specialist, you need expertise in medical terminology, pharmacovigilance processes, and a thorough understanding of the MedDRA dictionary, often supported by a degree in life sciences or healthcare. Familiarity with safety databases, MedDRA coding tools, and regulatory reporting systems is essential. Attention to detail, analytical thinking, and effective communication set top performers apart in this role. These skills ensure accurate adverse event coding, regulatory compliance, and high-quality safety data management in the pharmaceutical industry.

How does a MedDRA specialist typically collaborate with clinical and regulatory teams during the drug development process?

A MedDRA specialist plays a crucial role in ensuring accurate medical coding of adverse events and medical histories in clinical trials. They work closely with clinical research associates, data managers, and regulatory affairs professionals to standardize terminology and ensure compliance with regulatory requirements. Regular communication and collaboration are essential, as MedDRA specialists often provide guidance on coding conventions, review data for consistency, and help resolve complex coding queries. This cross-functional teamwork helps maintain data quality and supports timely regulatory submissions.

What is MedDRA and what is it used for?

MedDRA, which stands for Medical Dictionary for Regulatory Activities, is a standardized medical terminology system used globally to categorize and code medical information related to pharmaceuticals, such as adverse event reports, clinical trial data, and regulatory submissions. It helps ensure consistency and accuracy in how medical data is reported and analyzed across different countries and organizations. MedDRA is widely used by regulatory authorities, the pharmaceutical industry, and clinical research organizations to improve communication and safety monitoring in healthcare.

What is the difference between Meddra vs Medical Coder?

AspectMeddraMedical Coder
Required CredentialsTypically requires clinical terminology knowledge, coding experience, and sometimes certification in medical coding or terminologyRequires certification such as CPC, CCS, or CCS-P, with knowledge of medical coding standards
Work EnvironmentOften in healthcare settings, research, or pharmacovigilancePrimarily in hospitals, clinics, insurance companies, or coding service providers
Employer & Industry UsageUsed mainly in healthcare research, pharmacovigilance, and clinical data analysisUsed across healthcare providers, insurance companies, and coding agencies
Common Search & Comparison IntentUnderstanding differences in medical terminology coding systemsClarifying roles and certifications in medical coding

While Meddra focuses on standardized medical terminology for adverse event reporting, Medical Coders specialize in translating medical records into standardized codes for billing and documentation. Both roles require healthcare knowledge but serve different functions within the healthcare industry.

What are popular job titles related to Meddra jobs in Raleigh, NC? For Meddra jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Meddra jobs in Raleigh, NC look for? The top searched job categories for Meddra jobs in Raleigh, NC are:
Meddra jobs near you
Infographic showing various Meddra job openings in Raleigh, NC as of July 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 $51,529 per year, or $24.8 per hour.

Senior Medical Coder

Biodata Partners, Inc.

Raleigh, NC • On-site, Remote

$16 - $21.50/hr

Part-time

Re-posted 15 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)

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