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Meddra Coding Jobs in Maryland (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

Fort Detrick, MD · On-site

$85K - $105K/yr

MedDRA Certified and WHO-Drug Certified. * Minimum 7 years of medical coding experience . * Expertise with MedDRA and WHO Drug dictionaries. * Experience supporting FDA-regulated clinical studies.

VENESCO LLC

Medical Coder

Frederick, MD · On-site

$85K - $105K/yr

MedDRA Certified and WHO-Drug Certified. * Minimum 7 years of medical coding experience . * Expertise with MedDRA and WHO Drug dictionaries. * Experience supporting FDA-regulated clinical studies.

Venesco

Medical Coder

Frederick, MD · On-site

$18.75 - $24.75/hr

MedDRA Certified and WHO-Drug Certified. * Minimum 7 years of medical coding experience. * Expertise with MedDRA and WHO Drug dictionaries. * Experience supporting FDA-regulated clinical studies.

micro1 AI

Clinical Pharmacy Technicians

Baltimore, MD · Remote

$70 - $80/hr

Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness determination, and aggregate safety data analysis. * Expertise in reconciling aggregate safety data and ...

micro1 AI

Pharmacovigilance Expert

Baltimore, MD · Remote

$70 - $80/hr

Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness determination, and aggregate safety data analysis. * Expertise in reconciling aggregate safety data and ...

TRI Challenge Convention

S & P Associate

Bethesda, MD · Hybrid

Experienced Safety Associates are responsible for performing MedDRA coding and processing Serious Adverse Events (SAEs) to contribute to the development of comprehensive safety reports.Must have ...

Emmes

Senior 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 ...

All JobsMeddra Coding JobsMeddra Coding Jobs in Maryland

Meddra Coding information

See Maryland salary details

$8

$18

$28

How much do meddra coding jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for meddra coding in Maryland is $18.68, 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.

How do I get trained in Meddra coding?

Training for MedDRA coding typically involves completing specialized courses offered by organizations such as the Uppsala Monitoring Centre or through online platforms. These courses cover terminology, coding guidelines, and software tools, and often require prior knowledge of pharmacovigilance or medical terminology.

What is a MedDRA coding?

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, individuals typically complete relevant training in medical coding and gain experience in clinical documentation. Certification is often achieved through specialized programs or courses offered by industry organizations, and proficiency in coding tools and terminology is essential.

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, familiarity with medical concepts and use of coding tools can facilitate learning over time.
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Meddra Coding jobs near you
Infographic showing various Meddra Coding job openings in Maryland as of August 2026, with employment types broken down into 100% Full Time. Highlights an 80% In-person, and 20% Hybrid job distribution, with an average salary of $38,855 per year, or $18.7 per hour.

S & P Specialist

TRI Challenge Convention

Bethesda, MD • Hybrid

Full-time

Re-posted 18 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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