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Meddra Coding Jobs in California (NOW HIRING)

YO AI Labs

Pharmacovigilance Expert - Remote

San Jose, CA · Remote

$70 - $80/hr

MedDRA Coding * Seriousness & Causality Assessment * Expectedness Determination * Data Reconciliation * Regulatory Documentation * Structured Written Communication * Attention to Detail Preferred ...

JenaValve

Specialist, Clinical Safety

Irvine, CA · On-site

$100K/yr

Provide support to the MedDRA coding team on complex coding questions; participate in MedDRA coding team meetings and advise on important medical concepts. * Provide clinical and medical subject ...

Neurocrine Biosciences

Scientist, Safety

San Diego, CA

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... MedDRA coding of AEs, product labeling, Company Core Data Sheet (CCDS)) * Assist preparation of safety related regulatory submission documents including periodic and ad-hoc aggregate reports (eg ...

Neurocrine Biosciences, Inc.

Scientist, Safety

San Diego, CA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... MedDRA coding of AEs, product labeling, Company Core Data Sheet (CCDS)) * Assist preparation of safety related regulatory submission documents including periodic and ad-hoc aggregate reports (eg ...

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Meddra Coding information

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How much do meddra coding jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for meddra coding in California is $19.00, according to ZipRecruiter salary data. Most workers in this role earn between $11.15 and $26.35 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.

What are the most commonly searched types of Meddra Coding jobs in California?

The most popular types of Meddra Coding jobs in California are:

What are popular job titles related to Meddra Coding jobs in California?

For Meddra Coding jobs in California, the most frequently searched job titles are:

What job categories do people searching Meddra Coding jobs in California look for?

The top searched job categories for Meddra Coding jobs in California are:

What cities in California are hiring for Meddra Coding jobs?

Cities in California with the most Meddra Coding job openings:

Meddra Coding jobs near you
Infographic showing various Meddra Coding job openings in California as of August 2026, with employment types broken down into 89% Full Time, 7% Part Time, and 4% Contract. Highlights an 83% In-person, 4% Hybrid, and 13% Remote job distribution, with an average salary of $39,510 per year, or $19 per hour.

Pharmacovigilance Expert - Remote

YO AI Labs

Palo Alto, CA • Remote

Full-time

Posted 4 days ago

Job description

Job Title: Pharmacovigilance Expert

Job Type: Contractor
Location: Remote

Job Overview

We are seeking experienced Pharmacovigilance Experts to contribute their drug safety expertise to an innovative healthcare AI project. In this role, you will help improve next-generation AI systems by reviewing, evaluating, and refining pharmacovigilance documentation, safety reports, and regulatory content. No prior AI experience is required—your pharmacovigilance expertise, analytical skills, and commitment to data quality are what matter most.

Key Responsibilities

  • Author and review evaluation tasks based on DSURs, PSURs/PBRERs, safety data, and case-level records.

  • Assess safety findings, signal evaluations, and benefit-risk conclusions for accuracy and regulatory alignment.

  • Review reports for compliance with ICH E2F, ICH E2C(R2), and GVP guidelines.

  • Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources.

  • Evaluate safety conclusions based on new data, events, and regulatory requirements.

  • Provide structured written feedback and rationales to support AI-driven pharmacovigilance tools.

  • Ensure accuracy, completeness, and quality of regulatory safety documentation.

Required Skills

  • Pharmacovigilance

  • Drug Safety Report Authoring

  • DSUR/PSUR/PBRER Review

  • ICH E2F & ICH E2C(R2) Compliance

  • GVP Guidelines

  • Aggregate Safety Data Analysis

  • Signal Management

  • Benefit-Risk Assessment

  • MedDRA Coding

  • Seriousness & Causality Assessment

  • Expectedness Determination

  • Data Reconciliation

  • Regulatory Documentation

  • Structured Written Communication

  • Attention to Detail

Preferred Qualifications

  • 5+ years of pharmacovigilance or drug safety experience within a sponsor, CRO, or consulting environment.

  • Proven experience authoring or reviewing DSURs and/or PSURs/PBRERs.

  • Strong knowledge of ICH E2F, ICH E2C(R2), and GVP guidelines.

  • Hands-on experience with signal management, benefit-risk assessment, MedDRA coding, and safety data analysis.

  • Experience reconciling aggregate safety data with case-level information.

  • Advanced degree in life sciences, pharmacy, nursing, medicine, or related fields (PharmD, MD, MSc, or equivalent).

  • Experience in clinical development safety, post-marketing surveillance, QPPV/deputy QPPV roles, safety committees, or AI-assisted safety review tools is a plus.