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Meddra Coding Jobs (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 ...

Integrated Resources INC

Medical Coder

Cambridge, MA

$20.50 - $27.25/hr

Principal Accountabilities Perform medical coding (WHO Drug Dictionary Enhanced and MedDRA) activities maintaining optimal communication with SABR staff and SABR vendors for all post marketing cases ...

Integrated Resources INC

Medical Coder

Cambridge, MA

$20.50 - $27.25/hr

Perform medical coding (WHO Drug Dictionary Enhanced and MedDRA) activities according to the coding schedule. Maintain optimal communication with Safety staff and Safety vendors for all post ...

AstraZeneca

Director, Safety Scientist

Boston, MA · On-site

$175K - $263K/yr

Experience in MedDRA coding and search strategies * Excellent, independent judgment based on knowledge and expertise * Strong personal time-management and project-management skills * Mastery of ...

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Meddra Coding information

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How much do meddra coding jobs pay per hour?

As of Jun 28, 2026, the average hourly pay for meddra coding in the United States is $19.25, according to ZipRecruiter salary data. Most workers in this role earn between $11.30 and $26.68 per hour, depending on experience, location, and employer.

How do I get trained in MedDRA coding?

Training in MedDRA coding typically involves completing specialized courses offered by the MedDRA Maintenance and Support Services Organization (MSSO) or accredited training providers. These courses cover terminology, coding rules, and software tools, and often lead to certification that demonstrates proficiency in MedDRA coding standards.

What is the highest paid medical coder job?

Senior or specialized medical coders, such as those with credentials like Certified Professional Coder (CPC) or Certified Coding Specialist (CCS), tend to earn the highest salaries in medical coding. Positions involving coding for complex specialties like radiology, cardiology, or oncology often offer higher pay, especially with experience and advanced certifications.

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.

How to become a certified MedDRA coder?

To become a certified MedDRA coder, professionals typically complete training programs offered by the MedDRA Maintenance and Support Services Organization (MSSO) or authorized training providers, gaining knowledge of coding principles and terminology. Certification is often achieved through passing assessments that demonstrate proficiency in MedDRA coding, which may be required by employers in pharmacovigilance, clinical research, or regulatory roles.

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.

Is MedDRA coding difficult to learn?

MedDRA coding for medical coding professionals involves understanding complex medical terminology and classification systems, which can require dedicated training and practice. While some find it challenging initially, proficiency improves with experience, and many organizations offer training programs or certifications to facilitate learning.
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Meddra Coding jobs near you
Infographic showing various Meddra Coding job openings in the United States as of June 2026, with employment types broken down into 86% Full Time, 7% Part Time, and 7% Contract. Highlights an 60% In-person, 7% Hybrid, and 33% Remote job distribution, with an average salary of $40,035 per year, or $19.2 per hour.
S & P Specialist

S & P Specialist

Technical Resources International, Inc

Bethesda, MD • On-site

Full-time

Posted 7 days ago

Job description

Job Title
S & P Specialist
Location
Bethesda, MD 20817 US (Primary)
Category
Drug Safety
Job Type
Full-Time
Salary Range
70,000.00-85,000.00/YEAR
Education
Master's Degree
Travel
None
Job Description
  • Ensures compliance with TRI Standard Operating Procedures, Food and Drug Administration and World Health Organization regulations and global regulations for the reporting of adverse events to regulatory agencies
  • Develops and ensures the uniform and timely processing of adverse event reports
  • Provides medical evaluation of adverse event reports
  • Performs various tasks in support of clinical research including the reporting, collecting, and sharing of results and issues around adverse event reports both for currently marketed drugs as well as those in the experimental stages of development
  • Maintains/updates agent-specific clinical and preclinical toxicity study summary tables for investigational agents
  • Performs literature searches
  • Performs various tasks in support of clinical research including adverse event analysis and processing, serious adverse event reconciliation.
  • Preparation of IND safety reports for submission to the FDA; safety document or data analysis.
  • Clinical trial site support; reporting, collecting, and sharing of results and issues around adverse event reports both for currently marketed drugs as well as those in the experimental stages of development.
  • Assists in the preparation of new drug application safety updates, investigational new drug safety reports, investigator communication, product labeling/package inserts, and other reports as necessary.
  • May review experimental protocols and informed consent documents; and prepare, review, and edit presentations regarding safety issues.

Job Requirements
  • Knowledge of GCP and ICH guidelines preferred; drug development/clinical trial experience essential.
  • Knowledge of safety databases and/or MedDRA coding preferred.
  • Experience leading clinical and cross functional teams is a plus.
  • Must have excellent oral, written, presentation and computer skills.
  • 2+ years of academic, pharmaceutical or biotech industry or academic experience.
  • This is a hybrid position with 2 days in TRI's Bethesda, Maryland office, and 3 days working remotely.

We are equal opportunity/affirmative action employers, committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status, or any other protected characteristic under state or local law.

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