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Meddra Coding Jobs in Teaneck, NJ (NOW HIRING)

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Meddra Coding information

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$10

$21

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How much do meddra coding jobs pay per hour?

As of Sep 7, 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.

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.

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.

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.

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What job categories do people searching Meddra Coding jobs in Teaneck, NJ look for?

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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 33% Full Time, 33% Part Time, and 34% Contract. Highlights an 33% In-person, and 67% Remote job distribution, with an average salary of $44,134 per year, or $21.2 per hour.

Contractor - Principal Statistical Programmer

Scorpion Therapeutics

Manhattan, NY • On-site

$125 - $150/hr

Other

Posted 5 days ago


Job description

The Principal Statistical Programmer will provide expert-level hands-on programming support and technical expertise to develop, maintain, validate, and execute SAS programs that access, visualize, analyze, and report clinical trial data in accordance with statistical analysis plans, ICH guidelines, and applicable regulatory requirements. Supports statistical programming for in-house and outsourced clinical trials, commercial requests, HEOR analyses, pooled analyses (ISE/ISS), biomarker analyses, and ad hoc analyses.

Key Responsibilities:
  • Support study leads and take ownership of multiple deliverables across drug programs and platforms.
  • Act as an integral project team member, collaborating with vendors, biostatisticians, data managers, and cross-functional teams.
  • Primary role for production of tables, listings, and figures, and CRF tabulations (including ISS/ISE).
  • Serve as primary programmer for regulatory, commercial, ad hoc, biomarker, and HEOR analyses.
  • Review critical Standards Artifacts and Processes (e.g., SAPs, Data Validation Plans, eCRFs) and provide comments.
  • Troubleshoot and provide quality review of complex SAS programs; follow good programming practices and document programs.
  • Understand and follow FDA regulations affecting clinical trial data reporting.
Desired Experience/Education and Skills:
  • At least 8 years relevant experience (5+ years may be considered); Bachelor’s degree.
  • Oncology experience required; leukemia experience preferred.
  • Excellent communication to non-technical colleagues; completed large/complex projects; handle multiple projects with aggressive timelines.
  • Advanced/excellent SAS knowledge; familiarity with coding dictionaries (WHO, MedDRA); expert in CDISC.
  • Knowledge of medical/statistical terminology; capable with Windows, Word, and Excel.
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