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Meddra Coding Jobs in Washington (NOW HIRING)

TRI Challenge Convention

S & P Specialist

Bethesda, MD · Hybrid

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+ ...

VENESCO, LLC

Medical Coder

Falls Church, VA · On-site +1

$20 - $26.75/hr

Bachelor's degree in life sciences or related field 3-5 years of medical coding experience Knowledge of MedDRA and WHO Drug coding systems Preferred Qualifications: Medical coding certification ...

VENESCO LLC

Medical Coder

Falls Church, VA · On-site

$20 - $26.75/hr

... coding and reconciliation of medical data. Requirements: Key Responsibilities: • Code medical terminology using MedDRA and WHO Drug dictionaries • Ensure consistency and quality of coded clinical ...

Venesco LLC

Medical Coder

Falls Church, VA · On-site

$20 - $26.75/hr

... coding and reconciliation of medical data. Requirements Key Responsibilities: • Code medical terminology using MedDRA and WHO Drug dictionaries • Ensure consistency and quality of coded clinical ...

The Emmes Company, LLC

Medical Officer

Rockville, MD · Remote

Reviews and approves Medical Dictionary for Regulatory Activities (MedDRA) and WHO Drug coding. * Reviews the FDA MedWatch Alerts, safety communications and or other communications from other ...

Emmes

Medical Officer

Rockville, MD · Remote

Reviews and approves Medical Dictionary for Regulatory Activities (MedDRA) and WHO Drug coding. * Reviews the FDA MedWatch Alerts, safety communications and or other communications from other ...

The Emmes Company, LLC

Medical Officer

Rockville, MD · Remote

Reviews and approves Medical Dictionary for Regulatory Activities (MedDRA) and WHO Drug coding. * Reviews the FDA MedWatch Alerts, safety communications and or other communications from other ...

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Meddra Coding information

See Washington salary details

$10

$21

$33

How much do meddra coding jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for meddra coding in Washington is $21.80, according to ZipRecruiter salary data. Most workers in this role earn between $12.79 and $30.24 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 Washington? The most popular types of Meddra Coding jobs in Washington are:
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Meddra Coding jobs near you
Infographic showing various Meddra Coding job openings in Washington as of May 2026, with employment types broken down into 2% Internship, 2% As Needed, 26% Full Time, 67% Part Time, 2% Temporary, and 1% Nights. Highlights an 76% Physical, 4% Hybrid, and 20% Remote job distribution, with an average salary of $45,343 per year, or $21.8 per hour.

S & P Specialist

TRI Challenge Convention

Bethesda, MD • Hybrid

Full-time

Posted 17 days ago

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.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.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.

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