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Meddra Coder Jobs in California (NOW HIRING)

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How much do meddra coder jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for meddra coder in California is $22.13, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $23.70 per hour, depending on experience, location, and employer.

What are common challenges faced by MedDRA coders?

Meddra Coders often encounter challenges such as interpreting ambiguous or incomplete clinical data, ensuring consistency in coding across different studies, and keeping up with frequent updates to the MedDRA dictionary. They also need to collaborate closely with clinical and safety teams to clarify terminology and resolve discrepancies. Attention to detail and strong communication skills are essential to ensure data quality and regulatory compliance in this role.

What is the difference between Meddra Coder vs Medical Coder?

AspectMeddra CoderMedical Coder
CredentialsCertification in MedDRA coding, often through specialized trainingCertification like CPC or CCS, with focus on ICD, CPT, or HCPCS coding
Work EnvironmentPharmaceutical, clinical research, or healthcare settings focusing on adverse event reportingHospitals, clinics, insurance companies, and healthcare providers
Industry UsageUsed primarily in drug safety and pharmacovigilanceUsed broadly across healthcare for billing, documentation, and coding

While both Meddra Coder and Medical Coder work with medical coding, Meddra Coder specializes in coding adverse events and drug safety data using MedDRA terminology, whereas Medical Coders handle billing and documentation coding across various medical specialties. The roles differ mainly in their focus and industry applications.

What skills and qualifications are needed to be a MedDRA coder?

To thrive as a MedDRA Coder, you need a strong understanding of medical terminology, pharmacovigilance concepts, and experience with adverse event coding, often supported by a life sciences degree. Familiarity with MedDRA coding software, safety databases like Argus or ArisG, and relevant certifications such as MedDRA training are typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills for ensuring accurate classification and collaborating with clinical teams. These skills and qualifications are vital for maintaining data integrity, regulatory compliance, and the quality of safety reporting in clinical research and drug safety.

What is a MedDRA coder?

A MedDRA Coder is a professional responsible for assigning standardized Medical Dictionary for Regulatory Activities (MedDRA) terms to medical information such as adverse event reports, clinical trial data, and safety narratives. This ensures data consistency and facilitates regulatory reporting and pharmacovigilance activities within the pharmaceutical and healthcare industries. MedDRA Coders interpret clinical and medical terminology to accurately code data, helping organizations comply with global regulatory requirements. Their work is crucial for effective drug safety monitoring and communication with health authorities worldwide.

What are popular job titles related to Meddra Coder jobs in California?

For Meddra Coder jobs in California, the most frequently searched job titles are:

What job categories do people searching Meddra Coder jobs in California look for?

The top searched job categories for Meddra Coder jobs in California are:

What cities in California are hiring for Meddra Coder jobs?

Cities in California with the most Meddra Coder job openings:

Meddra Coder jobs near you
Infographic showing various Meddra Coder job openings in California as of August 2026, with employment types broken down into 83% Full Time, and 17% Contract. Highlights an 100% In-person job distribution, with an average salary of $46,027 per year, or $22.1 per hour.

Senior Specialist I, Postmarketing Patient Safety and Pharmacovigilance Operations

Corcept Therapeutics

Redwood City, CA

$103K - $137K/yr

Full-time

Re-posted 7 days ago

Job description

The role supports drug safety and pharmacovigilance activities in post-marketing setting focusing on supporting case management activities, particularly focused on the oversight of quality and compliance of vendor/service provider activities.

Responsibilities: 

  • Support the oversight of drug safety/pharmacovigilance service providers to ensure the collection, processing, reporting and reconciliation of adverse events reports in compliance with global regulatory requirements
  • Perform in line and/or end of line quality review of adverse event reports
  • Assists in the creation/revision of department standard operating procedures and work instructions
  • Development and delivery of training for safety related topics
  • Support process improvement initiatives and safety systems activities
  • Support and participate in audits and inspections, including preparation activities
  • Assist with safety operations and/or safety science activities and projects, as necessary

Required Skills, Qualifications and Technical Proficiencies:

  • Ability to work in a dynamic environment to meet patient and corporate needs
  • Knowledge of Argus (or similar safety applications) and MedDRA and WHO Drug coding dictionaries
  • Excellent communication and collaboration skills
  • Ability to manage multiple projects in a fast-paced environment

Education and Experience:

  • Bachelor's degree in healthcare or life sciences- degree such as RN or BSN, PharmD is preferred
  • Minimum of 3 years Patient Safety & Pharmacovigilance experience in a global environment
  • Experience in post marketing safety operations preferred
  • Working knowledge of FDA, EU and ICH guidelines for safety reporting and processing for clinical trials and post marketing

The pay range that the Company reasonably expects to pay for this position is $103,600 - $137,100; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.

 Applicants must be currently authorized to work in the United States on a full-time basis.

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