Core systems include AVISSO (Argus), Empirica Signals and Topics, Global Intake Tool, MedDRA Coding Tool, ICSR Reporting Rule Survey, RMS-RSI, SLARDS, and TransformPV. The candidate must understand ...
Core systems include AVISSO (Argus), Empirica Signals and Topics, Global Intake Tool, MedDRA Coding Tool, ICSR Reporting Rule Survey, RMS-RSI, SLARDS, and TransformPV. The candidate must understand ...
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 ...
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 ...
Specialist, Clinical Safety
Irvine, CA · On-site
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 ...
Specialist, Clinical Safety
Irvine, CA · On-site
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 ...
Drug Safety Associate I
Norwood, MA · Hybrid
Perform MedDRA and WHODrug coding for adverse events, indications, and suspect/concomitant medications. * Assess case seriousness, expectedness (per current IB/SmPC), and causality against source ...
Drug Safety Associate I
Norwood, MA · Hybrid
Perform MedDRA and WHODrug coding for adverse events, indications, and suspect/concomitant medications. * Assess case seriousness, expectedness (per current IB/SmPC), and causality against source ...
Drug Safety Associate I
Norwood, MA · On-site
Perform MedDRA and WHODrug coding for adverse events, indications, and suspect/concomitant medications. * Assess case seriousness, expectedness (per current IB/SmPC), and causality against source ...
Quick apply
Drug Safety Associate I
Norwood, MA · On-site
Perform MedDRA and WHODrug coding for adverse events, indications, and suspect/concomitant medications. * Assess case seriousness, expectedness (per current IB/SmPC), and causality against source ...
Assigns codes using MedDRA and WHODD terminologies, which most accurately describe each panel according to established coding guidelines and conventions. Performs reconciliation of safety report and ...
Assigns codes using MedDRA and WHODD terminologies, which most accurately describe each panel according to established coding guidelines and conventions. Performs reconciliation of safety report and ...
Medical Coder
Cambridge, MA · On-site
$20.50 - $27.25/hr
Perform medical coding (WHO Drug Dictionary Enhanced and MedDRA) activities according to the coding schedule. Maintain optimal communication with Safety staff and Safety vendors for all post ...
Medical Coder
Cambridge, MA · On-site
$20.50 - $27.25/hr
Perform medical coding (WHO Drug Dictionary Enhanced and MedDRA) activities according to the coding schedule. Maintain optimal communication with Safety staff and Safety vendors for all post ...
Drug Safety Associate I
Horsham, PA · On-site
Standard Operating Procedures and Working Instructions Department guidance documents MedDRA coding dictionary and MedDRA Points to Consider Understand relevant safety implications regarding contracts ...
Drug Safety Associate I
Horsham, PA · On-site
Standard Operating Procedures and Working Instructions Department guidance documents MedDRA coding dictionary and MedDRA Points to Consider Understand relevant safety implications regarding contracts ...
Director, Drug Safety - Pharmacovigilance
San Diego, CA · On-site
$180 - $280/hr
Strong knowledge of MedDRA, WHO Drug Dictionary and safety databases #J-18808-Ljbffr
Director, Drug Safety - Pharmacovigilance
San Diego, CA · On-site
$180 - $280/hr
Strong knowledge of MedDRA, WHO Drug Dictionary and safety databases #J-18808-Ljbffr
$186 - $279/hr
Performs review and approval of the MedDRA coding activities.* Maintains current knowledge of evolving pharmacovigilance regulations, industry standards, and best practices related to signal ...
New
$186 - $279/hr
Performs review and approval of the MedDRA coding activities.* Maintains current knowledge of evolving pharmacovigilance regulations, industry standards, and best practices related to signal ...
New
Oversee ICSR coding standards, ensuring consistent application of coding conventions (e.g., MedDRA and WHO Drug as applicable) and alignment with global standards and internal guidance. * Perform and ...
Oversee ICSR coding standards, ensuring consistent application of coding conventions (e.g., MedDRA and WHO Drug as applicable) and alignment with global standards and internal guidance. * Perform and ...
Associate Director, Global Medical Review
Princeton, KY · On-site
$186 - $279/hr
Performs review and approval of the MedDRA coding activities. * Maintains current knowledge of evolving pharmacovigilance regulations, industry standards, and best practices related to signal ...
New
Associate Director, Global Medical Review
Princeton, KY · On-site
$186 - $279/hr
Performs review and approval of the MedDRA coding activities. * Maintains current knowledge of evolving pharmacovigilance regulations, industry standards, and best practices related to signal ...
New
Senior Director, Drug Safety and Pharmacovigilance
San Francisco, CA · On-site
$300K - $375K/yr
MedDRA, WHODRL), ICH guidelines, and a working understanding of drug safety databases (e.g. ARGUS), effective project management skills, a demonstrated ability to provide critical and timely insight ...
Senior Director, Drug Safety and Pharmacovigilance
San Francisco, CA · On-site
$300K - $375K/yr
MedDRA, WHODRL), ICH guidelines, and a working understanding of drug safety databases (e.g. ARGUS), effective project management skills, a demonstrated ability to provide critical and timely insight ...
Associate Director, Safety Scientist Boston, Massachusetts, United States of America LGY_CDSU -[...]
Boston, MA · On-site
$126 - $190/hr
Strategizing and drafting of responses to regulatory inquiries on product safety issues inclusive of defining MedDRA search strategy* Representing GPS in global program teams and associated cross ...
Associate Director, Safety Scientist Boston, Massachusetts, United States of America LGY_CDSU -[...]
Boston, MA · On-site
$126 - $190/hr
Strategizing and drafting of responses to regulatory inquiries on product safety issues inclusive of defining MedDRA search strategy* Representing GPS in global program teams and associated cross ...
Associate Director, Safety Scientist
Boston, MA · On-site
$126K - $190K/yr
Strategizing and drafting of responses to regulatory inquiries on product safety issues inclusive of defining MedDRA search strategy * Representing GPS in global program teams and associated cross ...
Associate Director, Safety Scientist
Boston, MA · On-site
$126K - $190K/yr
Strategizing and drafting of responses to regulatory inquiries on product safety issues inclusive of defining MedDRA search strategy * Representing GPS in global program teams and associated cross ...
Associate Director, Global Medical Review
Princeton, NJ · On-site
$186 - $279/hr
Performs review and approval of the MedDRA coding activities.* Maintains current knowledge of evolving pharmacovigilance regulations, industry standards, and best practices related to signal ...
New
Associate Director, Global Medical Review
Princeton, NJ · On-site
$186 - $279/hr
Performs review and approval of the MedDRA coding activities.* Maintains current knowledge of evolving pharmacovigilance regulations, industry standards, and best practices related to signal ...
New
Associate Director, Safety Scientist
Boston, MA · On-site
$126K - $190K/yr
Strategizing and drafting of responses to regulatory inquiries on product safety issues inclusive of defining MedDRA search strategy * Representing GPS in global program teams and associated cross ...
Associate Director, Safety Scientist
Boston, MA · On-site
$126K - $190K/yr
Strategizing and drafting of responses to regulatory inquiries on product safety issues inclusive of defining MedDRA search strategy * Representing GPS in global program teams and associated cross ...
Associate Director, Safety Scientist
Boston, MA · On-site
$126K - $190K/yr
Strategizing and drafting of responses to regulatory inquiries on product safety issues inclusive of defining MedDRA search strategy * Representing GPS in global program teams and associated cross ...
Associate Director, Safety Scientist
Boston, MA · On-site
$126K - $190K/yr
Strategizing and drafting of responses to regulatory inquiries on product safety issues inclusive of defining MedDRA search strategy * Representing GPS in global program teams and associated cross ...
Associate Director, Safety Scientist
Boston, MA · On-site
$126K - $190K/yr
Strategizing and drafting of responses to regulatory inquiries on product safety issues inclusive of defining MedDRA search strategy * Representing GPS in global program teams and associated cross ...
Associate Director, Safety Scientist
Boston, MA · On-site
$126K - $190K/yr
Strategizing and drafting of responses to regulatory inquiries on product safety issues inclusive of defining MedDRA search strategy * Representing GPS in global program teams and associated cross ...
Performs review and approval of the MedDRA coding activities. * Maintains current knowledge of evolving pharmacovigilance regulations, industry standards, and best practices related to signal ...
Performs review and approval of the MedDRA coding activities. * Maintains current knowledge of evolving pharmacovigilance regulations, industry standards, and best practices related to signal ...
Meddra information
See salary details
$13.94 - $15.97
3% of jobs
$15.97 - $18.01
7% of jobs
$18.01 - $20.04
12% of jobs
$20.60 is the 25th percentile. Wages below this are outliers.
$20.04 - $22.07
11% of jobs
$22.07 - $24.10
15% of jobs
The median wage is $24.49 / hr.
$24.10 - $26.14
14% of jobs
$26.14 - $28.17
13% of jobs
$28.40 is the 75th percentile. Wages above this are outliers.
$28.17 - $30.20
12% of jobs
$30.20 - $32.23
7% of jobs
$32.23 - $34.27
4% of jobs
$34.27 - $36.30
3% of jobs
$13
$25
$36
How much do meddra jobs pay per hour?
What are the key skills and qualifications needed to thrive as a MedDRA specialist?
How does a MedDRA specialist typically collaborate with clinical and regulatory teams during the drug development process?
What is MedDRA?
What is the difference between Meddra vs Medical Coder?
| Aspect | Meddra | Medical Coder |
|---|---|---|
| Required Credentials | Typically requires clinical terminology knowledge, coding experience, and sometimes certification in medical coding or terminology | Requires certification such as CPC, CCS, or CCS-P, with knowledge of medical coding standards |
| Work Environment | Often in healthcare settings, research, or pharmacovigilance | Primarily in hospitals, clinics, insurance companies, or coding service providers |
| Employer & Industry Usage | Used mainly in healthcare research, pharmacovigilance, and clinical data analysis | Used across healthcare providers, insurance companies, and coding agencies |
| Common Search & Comparison Intent | Understanding differences in medical terminology coding systems | Clarifying roles and certifications in medical coding |
While Meddra focuses on standardized medical terminology for adverse event reporting, Medical Coders specialize in translating medical records into standardized codes for billing and documentation. Both roles require healthcare knowledge but serve different functions within the healthcare industry.
What states have the most Meddra jobs?
States with the most job openings for Meddra jobs include:
What job categories do people searching Meddra jobs look for?
The top searched job categories for Meddra jobs are:

Deloitte rating
8.2
Based on 92 frontline employees who took The Breakroom Quiz
44th of 150 rated financial services
Job description
Recruiting for this role ends on 9/11/2026
Work you'll do/Responsibilities
The Global Pharmacovigilance Functional QA Senior Consultant will Lead the onsite testing lead for Global Pharmacovigilance (GPV) tower - a 16-application portfolio covering the full PV case lifecycle from adverse event intake through signal detection and aggregate reporting. Core systems include AVISSO (Argus), Empirica Signals and Topics, Global Intake Tool, MedDRA Coding Tool, ICSR Reporting Rule Survey, RMS-RSI, SLARDS, and TransformPV. The candidate must understand the pharmacovigilance data flow and be comfortable leading client-facing interactions, driving UAT coordination, and ensuring release readiness in a GxP-regulated environment with zero-defect tolerance. Serve as the onsite testing lead for the GPV tower, acting as the primary interface between the testing team and GPV business stakeholders, project managers, and release governance forums. Develop and execute test strategy and plans for GxP-regulated PV applications in alignment with CSA/CSV methodology and Functional Risk Assessment (FRA) outcomes. Design and execute test scenarios across SIT, UAT, OQ, and PQ phases for safety database (AVISSO), signal detection (Empirica), intake (Global Intake Tool), coding (MedDRA), and reporting systems (ICSR Rules, SLARDS). Lead UAT coordination - scheduling, entry/exit criteria, business SME participation, and timely sign-off. Own defect lifecycle management including triage, root cause discussion, stakeholder communication, and closure. Prepare and present testing status reports, defect dashboards, and release readiness assessments to client stakeholders. Proactively escalate testing risks and issues with clear ownership and resolution timelines. Operate within ALM/ALVIS for test planning, execution tracking, and evidence capture. The successful candidate would possess these skills:
- Ability to work independently and collaborate as part of a team
- Effective written and verbal communication skills
- Meticulous attention to detail and quality of work product
- Ability to build and sustain professional relationships
- Ability to lead projects or workstreams
- Ability to manage and prioritize multiple tasks in a fast-paced and dynamic environment
- Strong interpersonal skills and professional demeanor
- Ability to meet deadlines
- Ability to provide clear guidance to others
AI & Engineering leverages cutting-edge engineering capabilities to build, deploy, and operate integrated/verticalized sector solutions in software, data, AI, network, and hybrid cloud infrastructure. These solutions are powered by engineering for business advantage, transforming mission-critical operations. We enable clients to stay ahead with the latest advancements by transforming engineering teams and modernizing technology & data platforms. Our delivery models are tailored to meet each client's unique requirements
Our Industry Solutions offering provides verticalized solutions that transform how clients sell products, deliver services, generate growth, and execute mission-critical operations. We deliver integrated business expertise with scalable, repeatable technology solutions specifically engineered for each sector.
Qualifications Required
- 5+ years of onsite testing for the GPV tower, acting as the primary interface between the testing team and GPV business stakeholders, project managers, and release governance forums.
- Develop and execute test strategy and plans for GxP-regulated PV applications in alignment with CSA/CSV methodology and Functional Risk Assessment (FRA) outcomes.
- Design and execute test scenarios across SIT, UAT, OQ, and PQ phases for safety database (AVISSO), signal detection (Empirica), intake (Global Intake Tool), coding (MedDRA), and reporting systems (ICSR Rules, SLARDS).
- Lead UAT coordination - scheduling, entry/exit criteria, business SME participation, and timely sign-off.
- Operate within ALM/ALVIS for test planning, execution tracking, and evidence capture.
- Bachelor's degree, preferably in information technology, business, or healthcare related field; or equivalent experience
- Limited immigration sponsorship may be available
- Ability to travel 10%, on average, based on the work you do and the clients and industries/sectors you serve
You may also be eligible to participate in a discretionary annual incentive program, subject to the rules governing the program, whereby an award, if any, depends on various factors, including, without limitation, individual and organizational performance.
Deloitte is committed to providing reasonable accommodations for people with disabilities. If you require a reasonable accommodation to participate in the recruiting process, please direct your inquiries to the Global Call Center (GCC) at USTalentCICInbox@deloitte.com.
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Benefits
At Deloitte, we know that great people make a great organization. We value our people and offer employees a broad range of benefits. Learn more about what working at Deloitte can mean for you.
Our people and culture
Our inclusive culture empowers our people to be who they are, contribute their unique perspectives, and make a difference individually and collectively. It enables us to leverage different ways of thinking, ideas, and perspectives, and bring more creativity and innovation to help solve our clients' most complex challenges. This makes Deloitte one of the most rewarding places to work.
Our purpose
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Professional development
From entry-level employees to senior leaders, we believe there's always room to learn. We offer opportunities to build new skills, take on leadership opportunities and connect and grow through mentorship. From on-the-job learning experiences to formal development programs, our professionals have a variety of opportunities to continue to grow throughout their career.
As used in this posting, "Deloitte" means Deloitte Consulting LLP, a subsidiary of Deloitte LLP. Please see https://www.deloitte.com/us/about for a detailed description of the legal structure of Deloitte LLP and its subsidiaries.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or protected veteran status, or any other legally protected basis, in accordance with applicable law.
Requisition code: 358936
Job ID 358936