ZipRecruiter

Log In

1

Meddra Coder 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 · 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 ...

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 ...

next page

Showing results 1-20

All JobsMeddra Coder JobsMeddra Coder Jobs in California

Meddra Coder information

See California salary details

$15

$22

$33

How much do meddra coder jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for meddra coder in California is $22.13, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $23.70 per hour, depending on experience, location, and employer.

What are common challenges faced by MedDRA coders?

Meddra Coders often encounter challenges such as interpreting ambiguous or incomplete clinical data, ensuring consistency in coding across different studies, and keeping up with frequent updates to the MedDRA dictionary. They also need to collaborate closely with clinical and safety teams to clarify terminology and resolve discrepancies. Attention to detail and strong communication skills are essential to ensure data quality and regulatory compliance in this role.

What is the difference between Meddra Coder vs Medical Coder?

AspectMeddra CoderMedical Coder
CredentialsCertification in MedDRA coding, often through specialized trainingCertification like CPC or CCS, with focus on ICD, CPT, or HCPCS coding
Work EnvironmentPharmaceutical, clinical research, or healthcare settings focusing on adverse event reportingHospitals, clinics, insurance companies, and healthcare providers
Industry UsageUsed primarily in drug safety and pharmacovigilanceUsed broadly across healthcare for billing, documentation, and coding

While both Meddra Coder and Medical Coder work with medical coding, Meddra Coder specializes in coding adverse events and drug safety data using MedDRA terminology, whereas Medical Coders handle billing and documentation coding across various medical specialties. The roles differ mainly in their focus and industry applications.

What skills and qualifications are needed to be a MedDRA coder?

To thrive as a MedDRA Coder, you need a strong understanding of medical terminology, pharmacovigilance concepts, and experience with adverse event coding, often supported by a life sciences degree. Familiarity with MedDRA coding software, safety databases like Argus or ArisG, and relevant certifications such as MedDRA training are typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills for ensuring accurate classification and collaborating with clinical teams. These skills and qualifications are vital for maintaining data integrity, regulatory compliance, and the quality of safety reporting in clinical research and drug safety.

What is a MedDRA coder?

A MedDRA Coder is a professional responsible for assigning standardized Medical Dictionary for Regulatory Activities (MedDRA) terms to medical information such as adverse event reports, clinical trial data, and safety narratives. This ensures data consistency and facilitates regulatory reporting and pharmacovigilance activities within the pharmaceutical and healthcare industries. MedDRA Coders interpret clinical and medical terminology to accurately code data, helping organizations comply with global regulatory requirements. Their work is crucial for effective drug safety monitoring and communication with health authorities worldwide.

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

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

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

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

What cities in California are hiring for Meddra Coder jobs?

Cities in California with the most Meddra Coder job openings:

Meddra Coder jobs near you
Infographic showing various Meddra Coder job openings in California as of August 2026, with employment types broken down into 83% Full Time, and 17% Contract. Highlights an 100% In-person job distribution, with an average salary of $46,027 per year, or $22.1 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.