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Remote Meddra Coding Jobs (NOW HIRING)

Pharmacovigilance Expert

Elgin, IL · Remote

$70 - $80/hr

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness ...

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Remote Meddra Coding information

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$23

How much do remote meddra coding jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for remote meddra coding in the United States is $21.50, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $22.84 per hour, depending on experience, location, and employer.

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.
More about Remote Meddra Coding jobs
What cities are hiring for Remote Meddra Coding jobs? Cities with the most Remote Meddra Coding job openings:
What are the most commonly searched types of Meddra Coding jobs? The most popular types of Meddra Coding jobs are:
What states have the most Remote Meddra Coding jobs? States with the most job openings for Remote Meddra Coding jobs include:
Infographic showing various Remote Meddra Coding job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 83% Full Time, 9% Part Time, and 6% Contract. Highlights an 78% Physical, 4% Hybrid, and 18% Remote job distribution, with an average salary of $44,724 per year, or $21.5 per hour.

Pharmacovigilance Expert

micro1 AI

Elgin, IL • Remote

$70 - $80/hr

Part-time

Posted 7 days ago


Job description

Role Title: Pharmacovigilance Expert


Role Type: Contractor


Location: Remote


micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters. This opportunity is ideal for professionals experienced in authoring and reviewing complex safety reports, passionate about data quality, and committed to clear written and verbal communication.


Scope of Work

  1. Author and review evaluation tasks based on DSURs, PSURs/PBRERs, and associated safety data and case-level records.
  2. Apply expert judgment to assess the accuracy and adequacy of interval safety findings, signal evaluations, and benefit-risk conclusions in alignment with best practices.
  3. Assess template and structural conformity to ICH E2F and ICH E2C requirements, including proper section content, presentation of cumulative versus interval data, and completeness of appendices.
  4. Reconcile figures and case counts across report sections and data sources, identifying and documenting discrepancies significant for regulatory review.
  5. Evaluate safety conclusions in light of new data or events, and provide clear, structured written rationales supporting your determinations.
  6. Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis.


Preferred Qualifications

  1. 5+ years of pharmacovigilance or drug safety experience at a sponsor, CRO, or as an independent consultant.
  2. Demonstrated proficiency in authoring or reviewing DSURs and/or PSURs/PBRERs from start to finish.
  3. Working fluency with ICH E2F, ICH E2C(R2), and GVP guidelines, including signal management and benefit-risk assessment methodology.
  4. Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness determination, and aggregate safety data analysis.
  5. Expertise in reconciling aggregate safety data and identifying inconsistencies with case-level information.
  6. Advanced degree in life sciences, pharmacy, nursing, or medicine (PharmD, MD, MSc, or equivalent).
  7. Experience in both development-stage and post-marketing safety reporting, QPPV or deputy QPPV roles, safety committee participation, or AI-assisted safety review tools is a plus.