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Meddra Whodrug Coding Jobs (NOW HIRING)

DaMar Staffing

Senior Medical Coder

Raleigh, NC · On-site

$18.25 - $24.25/hr

CTCAE coding and review Experience: * 5+ years in Pharmaceutical/Biotechnology industry or CRO environment * Thorough knowledge and experience with WHODrug AND MedDRA dictionaries * Knowledge of ICH ...

Biodata Partners, Inc.

Senior Medical Coder

Raleigh, NC · On-site +1

$16 - $21.50/hr

CTCAE coding and review Experience: * 5+ years in Pharmaceutical/Biotechnology industry or CRO environment * Thorough knowledge and experience with WHODrug AND MedDRA dictionaries * Knowledge of ICH ...

AA2IT

Medical Device Vigilance professionals

Raleigh, NC · On-site

$40 - $42/hr

This also includes MedDRA, WHODrug, and IMDRF coding. * Must work effectively/collaboratively in a fast-paced yet efficient team environment with individuals at all levels within an organization.

Jobless

$165K - $179K/yr

Strong knowledge of MedDRA and WHODrug coding conventions. * Excellent written and verbal communication skills, with the ability to convey complex information clearly and concisely. * Strong ...

Celcuity Inc.

Strong knowledge of MedDRA and WHODrug coding conventions. * Excellent written and verbal communication skills, with the ability to convey complex information clearly and concisely. * Strong ...

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Meddra Whodrug Coding information

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How much do meddra whodrug coding jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for meddra whodrug coding in the United States is $20.67, according to ZipRecruiter salary data. Most workers in this role earn between $19.47 and $22.36 per hour, depending on experience, location, and employer.

What is MedDRA and WHO Drug coding?

MedDRA (Medical Dictionary for Regulatory Activities) and WHO Drug coding are standardized coding systems used in clinical research to classify medical terms and medications, respectively. MedDRA is used to code adverse events, medical history, and other clinical information, ensuring consistency and accuracy in data reporting. WHO Drug coding is applied to classify and standardize drug names and medicinal products. Both coding systems are essential for regulatory submissions, pharmacovigilance, and facilitating global data exchange. Accurate coding helps in the analysis and interpretation of clinical trial data.

What skills and qualifications are needed to thrive as a MedDRA/WHO Drug coder?

To thrive as a MedDRA/WHO Drug Coder, you need a solid understanding of medical terminology, pharmacology, and clinical data management, often supported by a life sciences degree or relevant experience. Familiarity with coding dictionaries like MedDRA and WHO Drug, as well as electronic data capture (EDC) systems and coding software, is essential. Attention to detail, analytical thinking, and strong communication skills help coders interpret clinical data accurately and resolve discrepancies. These skills are vital to ensure precise and consistent coding, which supports regulatory compliance and the integrity of clinical trial data.

What are common challenges faced by MedDRA/WHO Drug coders, and how can they be addressed?

Meddra/WHO Drug Coders often encounter challenges such as interpreting ambiguous medical terms or incomplete case information, which can make accurate coding difficult. To address these issues, coders should maintain open communication with clinical teams for clarification and stay updated on the latest MedDRA and WHO Drug Dictionary coding guidelines. Regular training and reviewing case studies can also help improve accuracy and efficiency, ensuring consistent and high-quality data for regulatory submissions.

What is the difference between Meddra Whodrug Coding vs Medical Coder?

AspectMeddra Whodrug CodingMedical Coder
CredentialsTypically requires knowledge of MedDRA and coding standardsRequires certification like CPC or CCS
Work EnvironmentPharmaceutical, clinical research, regulatory agenciesHospitals, clinics, insurance companies
Industry UsageUsed for adverse event reporting and drug safetyUsed for medical record documentation and billing

While both roles involve coding, Meddra Whodrug Coders focus on drug safety and adverse event classification using MedDRA standards, primarily in research and regulatory settings. Medical Coders handle patient records and billing in healthcare facilities. The roles differ in focus, environment, and required certifications, though both require strong attention to detail and knowledge of coding systems.

Infographic showing various Meddra Whodrug Coding job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 84% Full Time, 9% Part Time, and 5% Contract. Highlights an 75% Physical, 4% Hybrid, and 21% Remote job distribution, with an average salary of $42,984 per year, or $20.7 per hour.

Associate Medical Director, Medical Safety (California)

California, MD • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

Full-time

Medical, Dental, Vision, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

Responsibilities:
  • Implement global safety strategy and monitor overall safety profile for investigational and marketed products throughout lifecycle.
  • Generate pre- and post-marketing safety deliverables (signal detection, benefit-risk evaluation, risk management).
  • Interface cross-functionally and with external Regulatory Authorities.
  • Manage safety assessment activities: review aggregate safety analyses/scientific literature, prepare safety reports, and communicate changes in product risk profile.
  • Provide Medical Safety/PV inputs to clinical development, investigator-sponsored programs, compassionate use, and disease monitoring programs; liaise with study and safety stakeholders (Clinical Sciences/Operations, Medical Affairs, Biometrics, Regulatory Affairs, CROs, DMCs).
  • Support global launch activities with PV/medical safety inputs.
  • Prepare/review safety sections for clinical, regulatory, and scientific documents (protocols, consent forms, CRFs, statistical plans, clinical study reports/synopses, integrated safety summaries, NDA/BLA, MAA, CTD submissions, regulatory responses, IRB/EC requests, briefing books, manuscripts).
  • Maintain Company Core Safety Information (CCSI) implementation across RSI/labeling; review relevant literature for signals.
  • Conduct signal detection, evaluation, validation, and communicate safety assessments.
  • Chair Safety Management Team (SMT); oversee preparation/review of aggregate safety reports (PSUR/PBRER, PADER, DSUR, IND Annual Reports, 6-month SUSAR line listings).
  • Contribute to Risk Management Plans (RMPs); guide MedDRA/WHODrug coding.
  • Ensure compliance with PV regulations/guidelines and support audits/inspections.
  • Represent PV in cross-functional forums; contribute to PV KPIs; stay current on PV guidance.
Required:
  • MD (or equivalent); medical licensure in at least one state preferred.
  • Minimum 3 years Drug Safety/Pharmacovigilance or 3+ years clinical development.
Required Skills/Abilities:
  • Working knowledge of global PV regulatory environment and Good Pharmacovigilance Practices (GVP).
  • Working knowledge of safety databases (e.g., ARISg/ARGUS) and electronic data capture.
  • MedDRA training and coding dictionary knowledge.
  • Ability to manage multiple deadlines; strong written/oral communication and cross-functional teamwork.
  • Computer literacy (Regulatory databases, Excel, PowerPoint, Word); some travel possible.
Benefits (US candidates):
  • medical/dental/vision insurance, 401(k), flexible paid vacation; discretionary bonus/incentive and potential equity grants.
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