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Remote Meddra Coding Jobs in California (NOW HIRING)

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Remote Meddra Coding information

What are some common challenges faced by professionals in remote MedDRA coding roles, and how can they be addressed?

Remote MedDRA coders often face challenges such as maintaining data consistency across different projects, staying updated with regular MedDRA version changes, and effectively communicating with global pharmacovigilance or clinical teams. To address these, it's important to follow established coding guidelines, participate in ongoing training, and use collaboration tools for regular check-ins with team members. Proactively seeking clarification and documenting coding decisions can also help ensure accuracy and support team alignment.

What is remote MedDRA coding?

Remote MedDRA coding involves assigning standardized medical terminology codes from the MedDRA (Medical Dictionary for Regulatory Activities) system to medical information, such as adverse event reports, from a remote location. This process helps ensure consistency and accuracy in the reporting of medical data for regulatory submissions and pharmacovigilance. Remote MedDRA coders typically work for pharmaceutical companies, CROs, or regulatory agencies, reviewing clinical data and using specialized software to code terms according to MedDRA guidelines.

What is the difference between Remote Meddra Coding vs Remote Medical Coding?

AspectRemote Meddra CodingRemote Medical Coding
CertificationsMedDRA certification, coding credentialsAHIMA or AAPC medical coding certifications
Work EnvironmentRemote, healthcare, pharmaceutical, or clinical research settingsRemote, healthcare facilities, insurance companies, or billing services
Industry UsagePharmaceuticals, clinical trials, regulatory agenciesHospitals, clinics, insurance companies, billing companies
Search & Comparison IntentUnderstanding specialized coding for drug safety and regulatory purposesGeneral medical billing and coding for healthcare providers

Remote Meddra Coding focuses on coding for drug safety and regulatory submissions using MedDRA standards, often in pharmaceutical or clinical research contexts. Remote Medical Coding covers a broader range of medical billing and coding tasks for healthcare providers. While both roles require coding certifications, their industry applications and work environments differ, making each role specialized for distinct healthcare and regulatory needs.

What are the key skills and qualifications needed to thrive as a remote MedDRA coder?

To thrive as a Remote MedDRA Coder, you need a strong background in life sciences or healthcare, familiarity with medical terminology, and experience in pharmacovigilance or clinical data management. Proficiency with MedDRA coding software, safety databases (such as Argus or Oracle), and relevant certifications like MedDRA training are commonly required. Attention to detail, analytical thinking, and effective written communication help ensure accurate and consistent medical coding. These skills and qualifications are essential for maintaining data quality, regulatory compliance, and supporting patient safety in clinical research and drug safety reporting.

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

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

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

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

What cities in California are hiring for Remote Meddra Coding jobs?

Cities in California with the most Remote Meddra Coding job openings:

Remote Meddra Coding jobs near you
Infographic showing various Remote Meddra Coding job openings in California as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 81% Full Time, 10% Part Time, 2% Temporary, and 5% Contract. Highlights an 78% Physical, 4% Hybrid, and 18% Remote job distribution.

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.