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Meddra Coding Jobs in California (NOW HIRING)

Exelixis

Associate Clinical Data Management Director

Alameda, CA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Manage data transfers with CROs and third-party data sources, SAE/AE reconciliation and MedDRA /WHO-DD coding. * Support the transfer, locking, and archiving of study databases. Manage scheduling and ...

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How much do meddra coding jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for meddra coding in California is $19.00, according to ZipRecruiter salary data. Most workers in this role earn between $11.15 and $26.35 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 the most commonly searched types of Meddra Coding jobs in California?

The most popular types of Meddra Coding jobs in California are:

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

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

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

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

What cities in California are hiring for Meddra Coding jobs?

Cities in California with the most Meddra Coding job openings:

Meddra Coding jobs near you
Infographic showing various Meddra Coding job openings in California as of August 2026, with employment types broken down into 89% Full Time, 7% Part Time, and 4% Contract. Highlights an 83% In-person, 4% Hybrid, and 13% Remote job distribution, with an average salary of $39,510 per year, or $19 per hour.

Senior Specialist I, Postmarketing Patient Safety and Pharmacovigilance Operations

Corcept Therapeutics

Redwood City, CA • On-site

$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.

Apply