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 ...
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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 ...
... coding system (e.g. ICD, CPT, HCPCS, LOINC, MedDRA) and delivery system (e.g payers and reimbursement models) Experience conducting routine and advanced statistical analyses for RWE generation ...
... coding system (e.g. ICD, CPT, HCPCS, LOINC, MedDRA) and delivery system (e.g payers and reimbursement models) Experience conducting routine and advanced statistical analyses for RWE generation ...
Meddra Coding information
See Connecticut salary details
$8.69 - $10.48
21% of jobs
$10.85 is the 25th percentile. Wages below this are outliers.
$10.48 - $12.27
20% of jobs
$12.27 - $14.05
8% of jobs
The median wage is $14.41 / hr.
$14.05 - $15.84
5% of jobs
$15.84 - $17.63
0% of jobs
$17.63 - $19.42
0% of jobs
$19.42 - $21.20
0% of jobs
$21.20 - $22.99
9% of jobs
$24.78 is the 75th percentile. Wages above this are outliers.
$22.99 - $24.78
11% of jobs
$24.78 - $26.57
13% of jobs
$26.57 - $28.36
13% of jobs
$8
$18
$28
How much do meddra coding jobs pay per hour?
As of Jul 27, 2026, the average hourly pay for meddra coding in Connecticut is $18.31, according to ZipRecruiter salary data. Most workers in this role earn between $10.77 and $25.38 per hour, depending on experience, location, and employer.
How do I get trained in MedDRA coding?
Training in MedDRA coding typically involves completing specialized courses offered by the MedDRA Maintenance and Support Services Organization (MSSO) or accredited training providers. These courses cover terminology, coding procedures, and software tools, and often require a basic understanding of pharmacovigilance or medical terminology. Certification or completion of training can enhance proficiency and job prospects in MedDRA coding roles.
What is a MedDRA Coding job?
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 training programs offered by the MedDRA Maintenance and Support Services Organization (MSSO) or authorized providers, gaining knowledge of coding principles and terminology. Certification often involves passing an exam that tests understanding of MedDRA coding rules and application, and maintaining proficiency may require ongoing education or recertification. Strong attention to detail and familiarity with medical terminology are essential for success in this role.
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 medical coder gets paid the most?
Senior medical coders, such as Certified Professional Coders (CPC) with specialized expertise or those working in high-demand settings like hospitals or specialty clinics, tend to earn the highest salaries. Experience, certifications, and proficiency with coding tools like ICD-10 and CPT contribute to higher pay in the medical coding field.
What are popular job titles related to Meddra Coding jobs in Connecticut? For Meddra Coding jobs in Connecticut, the most frequently searched job titles are:
What job categories do people searching Meddra Coding jobs in Connecticut look for? The top searched job categories for Meddra Coding jobs in Connecticut are:
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