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Meddra Coding Jobs in New York (NOW HIRING)

micro1 AI

Clinical Pharmacy Technicians

Stamford, CT · Remote

$70 - $80/hr

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

micro1 AI

Pharmacovigilance Expert

Jersey City, NJ · Remote

$70 - $80/hr

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

micro1 AI

Clinical Pharmacy Technicians

Newark, NJ · Remote

$70 - $80/hr

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

micro1 AI

Pharmacovigilance Expert

Elizabeth, NJ · Remote

$70 - $80/hr

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

micro1 AI

Pharmacovigilance Expert

Yonkers, NY · Remote

$70 - $80/hr

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

micro1 AI

Pharmacovigilance Expert

New York, NY · Remote

$70 - $80/hr

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

micro1 AI

Clinical Pharmacy Technicians

New York, NY · Remote

$70 - $80/hr

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

micro1 AI

Pharmacovigilance Expert

Stamford, CT · Remote

$70 - $80/hr

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

micro1 AI

Pharmacovigilance Expert

Paterson, NJ · Remote

$70 - $80/hr

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

micro1 AI

Clinical Pharmacy Technicians

Yonkers, NY · Remote

$70 - $80/hr

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

micro1 AI

Clinical Pharmacy Technicians

Elizabeth, NJ · Remote

$70 - $80/hr

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

micro1 AI

Clinical Pharmacy Technicians

Jersey City, NJ · Remote

$70 - $80/hr

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

micro1 AI

Clinical Pharmacy Technicians

Paterson, NJ · Remote

$70 - $80/hr

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

micro1 AI

Pharmacovigilance Expert

Newark, NJ · Remote

$70 - $80/hr

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

Parexel

Senior RWE/RWA Programmer

New Brunswick, NJ · On-site +1

Familiarity with US and global healthcare coding systems (e.g., ICD, CPT, HCPCS, LOINC, MedDRA) * And healthcare delivery systems (e.g., payers and reimbursement models) * Experience conducting ...

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Meddra Coding information

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How much do meddra coding jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for meddra coding in New York is $21.06, according to ZipRecruiter salary data. Most workers in this role earn between $12.36 and $29.18 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.
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Meddra Coding jobs near you
Infographic showing various Meddra Coding job openings in New York as of July 2026, with employment types broken down into 1% Internship, 81% Full Time, 9% Part Time, 3% Temporary, and 6% Contract. Highlights an 79% Physical, 4% Hybrid, and 17% Remote job distribution, with an average salary of $43,799 per year, or $21.1 per hour.

Drug Safety Operations Associate

The Rockridge Group

Stamford, CT

Full-time

Re-posted 13 days ago

Job description

TITLE: Drug Safety Operations Associate
LOCATION: Stamford, CT
DURATION: 12 months
Job Description:
  • Position performs adverse event processing and submission responsibilities supporting the Case Management function within Drug Safety Operations.
Primary Responsibilities
  • Perform case processing activities (triage, data entry, report distribution) as required
    • Assess, process, and data enter all AE case types to meet compliance requirements
    • Perform triage on all case types to determine prioritization (if requested by Purdue)
    • Identify adverse events, seriousness, and listed Ness / labeled Ness for case assessment; review additional incoming information to determine reportability
    • Select the appropriate as reported causality and company causality
    • Perform all appropriate coding using MedDRA, WHO-DRUG, and Company Product dictionaries.
    • Own case narrative - create narrative text as required for medical orientation
    • Determine follow-up requirements and request follow-up as appropriate (e-mail, phone call, letter, etc.) to request additional information
    • Support ICSR submissions and transmissions as needed.
    • Perform CRO case QC activities, reconciliation etc as required.
    • Work on highest priority or assigned cases using Workflow Management System, or as directed
    • Participate in inspections and audits as identified, including interviews and provision of requested data
    • Meet KPIs/KQIs as designated by Purdue and in compliance with company guidelines and policies
    • Assist in writing late ICSR related deviations and CAPAs, upon request
    • Perform additional tasks as assigned. Work independently, assess matters, propose resolutions, and appropriately escalate internally within Purdue organization
Education and Experience Requirements:
  • Bachelor’s degree (advanced degree preferred) in life science or healthcare (e.g. nursing, pharmacy)
  • Five (5+) years of experience in a pharmaceutical/biopharmaceutical company
  • Three (3+) years in Drug Safety Operations role;
  • Experience overseeing CRO teams of case processors preferred
  • US FDA pharmacovigilance inspection experience preferred
Necessary Knowledge, Skills, and Abilities:
  • Resource and workflow management (monitoring and assigning tasks)
  • Up-to-date knowledge of US and international PV regulations and best practices
  • MedDRA coding
  • Considers present and future impacts when making recommendations
  • Strong negotiation and problem-solving skills
  • Analytical skills and attention to detail
  • Accountability – takes ownership of deliverables
Necessary Knowledge, Skills, and Abilities:
  • Resource and workflow management (monitoring and assigning tasks)
  • Up-to-date knowledge of US and international PV regulations and best practices
  • MedDRA coding
  • Considers present and future impacts when making recommendations
  • Strong negotiation and problem-solving skills
  • Analytical skills and attention to detail
  • Accountability – takes ownership of deliverables