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Meddra Coding Jobs in California (NOW HIRING)

JenaValve

Specialist, Clinical Safety

Irvine, CA · On-site

$100K/yr

Provide support to the MedDRA coding team on complex coding questions; participate in MedDRA coding team meetings and advise on important medical concepts. * Provide clinical and medical subject ...

Exelixis

Drug Safety Associate II - Study Ops

Alameda, CA · On-site

$116K - $165K/yr

MedDRA coding of SAEs and AEs as reported in source documents of SAE reports and development/revision of Exelixis MedDRA Coding Conventions to ensure consistent data categorization. * Defining and ...

Exelixis

Drug Safety Associate II - Study Ops

Alameda, CA · On-site

$116K - $165K/yr

MedDRA coding of SAEs and AEs as reported in source documents of SAE reports and development/revision of Exelixis MedDRA Coding Conventions to ensure consistent data categorization. * Defining and ...

Ardelyx

Medical Director, Pharmacovigilance

Newark, CA · On-site

$240K - $320K/yr

Proven ability to utilize MedDRA and assign appropriate MedDRA terms to describe adverse events and WHO DD dictionary coding to accurately capture and standardize information related to medicinal ...

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Meddra Coding information

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How much do meddra coding jobs pay per hour?

As of Jun 29, 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 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 rules, and software tools, and often lead to certification that demonstrates proficiency in MedDRA coding standards.

What is the highest paid medical coder job?

Senior or specialized medical coders, such as those with credentials like Certified Professional Coder (CPC) or Certified Coding Specialist (CCS), tend to earn the highest salaries in medical coding. Positions involving coding for complex specialties like radiology, cardiology, or oncology often offer higher pay, especially with experience and advanced certifications.

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, professionals typically complete training programs offered by the MedDRA Maintenance and Support Services Organization (MSSO) or authorized training providers, gaining knowledge of coding principles and terminology. Certification is often achieved through passing assessments that demonstrate proficiency in MedDRA coding, which may be required by employers in pharmacovigilance, clinical research, or regulatory roles.

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, proficiency improves with experience, and many organizations offer training programs or certifications to facilitate learning.
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Meddra Coding jobs near you
Infographic showing various Meddra Coding job openings in California as of June 2026, with employment types broken down into 85% Full Time, 9% Part Time, and 6% Contract. Highlights an 68% In-person, 6% Hybrid, and 26% Remote job distribution, with an average salary of $39,510 per year, or $19 per hour.
Specialist, Clinical Safety

Specialist, Clinical Safety

JenaValve

Irvine, CA • On-site

$100K/yr

Full-time

Posted 7 hours ago

Key responsibilities

  • Conduct assessments of adverse events and complaints across multiple clinical studies, perform complaint handling assessments, and report adverse events per regulatory requirements and trial safety processes.

  • Review and analyze aggregate safety reports to identify early safety signals and escalate findings to leadership with recommended next steps.

  • Interact with investigational sites and field monitors to obtain additional pertinent information on Case Report Forms and medical documentation.

Job description

Job Title: Specialist, Clinical Safety
Role Level: Individual Contributor (IC)
Supervisor/Manager Title: Senior Manager, Clinical Safety
Job Location & Environment: Irvine, CA - Corporate Office
Job Description Summary: Reporting to the Senior Manager, Clinical Safety, the Specialist, Clinical Safety supports the conduct and timely execution of JenaValve clinical trials by monitoring subject safety, ensuring accurate and compliant adverse event data reporting in clinical databases, and contributing to the review and analysis of clinical safety data. The role collaborates closely with cross-functional teams including Project Management, Field Monitoring, Regulatory Affairs, and the Case Review Board to maintain the quality and integrity of safety data collected across all active trials, including the ALIGN-AR Pivotal Trial, JENA-VAD Registry, ALIGN-AR EFS Trial, and the ARTIST Trial.
Job Responsibilities:
  • Conduct assessments of adverse events (AEs) and complaints across multiple clinical studies, including UADE (Unanticipated Adverse Device Effect) determinations; perform complaint handling assessments and report AEs per regulatory requirements, trial safety processes, and JenaValve procedures.
  • Review and analyze aggregate safety reports to identify early safety signals; escalate findings to leadership with recommended next steps.
  • Track timeliness of AE and SAE reporting by investigational sites and follow up as needed to ensure compliance with protocol-specified timelines.
  • Interact with investigational sites and field monitors to obtain additional pertinent information on Case Report Forms and medical documentation (source documents).
  • Manage, prepare, and review event narratives for internal review or external reviews (e.g., Clinical Events Committee, Data Safety Monitoring Board) and for regulatory submissions.
  • Provide support to the MedDRA coding team on complex coding questions; participate in MedDRA coding team meetings and advise on important medical concepts.
  • Provide clinical and medical subject matter expertise to address safety-related questions from internal study teams, field support personnel, monitors, and study sites during the conduct of studies.
  • Contribute to clinical aspects of protocol development; specifically develop the Safety section of clinical trial protocols including adverse event definitions, AE reporting requirements, and risk sections.
  • Collaborate with data management and cross-functional teams on the development of case report forms, study-specific safety reports, and other study forms, ensuring alignment with clinical definitions and EDC data flows.
  • Support DSMB and CEC startup and management activities including vendor selection and approval, member selection, charter development, and ongoing conduct during clinical trials.
  • Lead site CRF development for AE Main Forms and AE Sub-forms; review edit checks and provide input into other CRF form development as needed.
  • Support PMA/APR activities including query closure, case narratives, and accurate presentation of endpoint-related data.
  • Assist the Clinical Safety team in daily safety reviews, data reconciliation, periodic reporting, and identification of necessary source documents.
  • Contribute to other clinical and medical affairs activities as needed and support continuous process improvement.
  • Complete training for internal SOPs and maintain current knowledge required for the role.

Required Education and Experience:
  • 2+ years of experience in clinical trial research required; medical device experience strongly preferred.
  • Bachelor's degree or higher in a life sciences, health sciences, or related field required; advanced clinical degree (NP, PA, MD, or international equivalent) highly preferred.
  • Working knowledge of HIPAA, ICH, GCP, and regulatory requirements related to clinical research.
  • Experience with cardiovascular or structural heart therapeutic areas is a significant advantage.
  • Strong organizational skills and time management abilities in a dynamic, fast-paced environment; ability to manage multiple concurrent priorities.
  • Excellent critical thinking skills and strong written and verbal communication skills.
  • Self-motivated, detail-oriented, and able to work independently as well as part of a collaborative team.

Skills and Abilities Required for This Job:
  • Clinical knowledge in cardiology; structural heart disease or transcatheter valve therapy experience preferred.
  • Knowledge of GCPs governing clinical trial conduct; working knowledge of medical device regulations and ICH guidelines.
  • Experience working across all phases of clinical study conduct from a clinical safety perspective.
  • Familiarity with MedDRA coding, adverse event terminology, and safety database management.
  • Experience with EDC (Electronic Data Capture) platforms for clinical trial management and safety reporting.
  • Basic understanding of clinical trial design and statistical concepts as applied to safety evaluation.
  • Ability to work collaboratively as part of a multi-functional medical device development team.
  • Excellent oral and written communication skills; strong interpersonal skills and ability to work effectively cross-functionally and cross-culturally.
  • Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook).

Physical Requirements:
  • Standard office environment requirements.
  • Minimal travel, up to 10%.

Apply