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Meddra Coding Jobs in Teaneck, NJ (NOW HIRING)

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

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

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

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

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

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

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

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

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

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

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

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

Meddra Coding information

See Teaneck, NJ salary details

$10

$21

$32

How much do meddra coding jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for meddra coding in Teaneck, NJ is $21.22, according to ZipRecruiter salary data. Most workers in this role earn between $12.45 and $29.42 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 popular job titles related to Meddra Coding jobs in Teaneck, NJ? For Meddra Coding jobs in Teaneck, NJ, the most frequently searched job titles are:
What cities near Teaneck, NJ are hiring for Meddra Coding jobs? Cities near Teaneck, NJ with the most Meddra Coding job openings:
Infographic showing various Meddra Coding job openings in Teaneck, NJ as of August 2026, with employment types broken down into 100% Contract. Highlights an 100% In-person job distribution, with an average salary of $44,134 per year, or $21.2 per hour.

Pharmacovigilance Expert - Remote

YO AI Labs

New York, NY • Remote

Full-time

Posted 3 days ago

New


Job description

Job Title: Pharmacovigilance Expert

Job Type: Contractor
Location: Remote

Job Overview

We are seeking experienced Pharmacovigilance Experts to support an AI healthcare project by reviewing drug safety documentation, evaluating regulatory content, and improving AI-generated outputs. No AI experience is required—your pharmacovigilance expertise is what matters.

Key Responsibilities
  • Review and author DSURs, PSURs/PBRERs, and safety reports.
  • Evaluate safety signals and benefit-risk assessments.
  • Ensure compliance with ICH E2F, ICH E2C(R2), and GVP guidelines.
  • Analyze aggregate safety data and reconcile case information.
  • Review MedDRA coding, causality, seriousness, and expectedness.
  • Provide structured feedback to improve AI-generated content.
  • Maintain high standards of quality and regulatory compliance.
Required Skills
  • Pharmacovigilance
  • Drug Safety
  • DSUR/PSUR/PBRER Review
  • ICH E2F & ICH E2C(R2)
  • GVP Guidelines
  • Signal Management
  • Benefit-Risk Assessment
  • MedDRA Coding
  • Safety Data Analysis
  • Regulatory Documentation
  • Strong Written Communication
  • Attention to Detail
Preferred Qualifications
  • 5+ years of pharmacovigilance or drug safety experience.
  • Experience with DSURs, PSURs/PBRERs, and aggregate safety reports.
  • Strong knowledge of ICH E2F, ICH E2C(R2), and GVP.
  • Experience with signal management and safety data review.
  • Degree in Pharmacy, Medicine, Nursing, Life Sciences, or related field.
  • Experience in clinical safety, post-marketing surveillance, or CRO/pharmaceutical environments is a plus.