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Meddra Jobs (NOW HIRING)

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 ...

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 ...

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 ...

$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 ...

Showing results 41-60

Meddra information

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$13

$25

$36

How much do meddra jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for meddra in the United States is $25.49, according to ZipRecruiter salary data. Most workers in this role earn between $20.67 and $29.09 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a MedDRA specialist?

To thrive as a MedDRA Specialist, you need expertise in medical terminology, pharmacovigilance processes, and a thorough understanding of the MedDRA dictionary, often supported by a degree in life sciences or healthcare. Familiarity with safety databases, MedDRA coding tools, and regulatory reporting systems is essential. Attention to detail, analytical thinking, and effective communication set top performers apart in this role. These skills ensure accurate adverse event coding, regulatory compliance, and high-quality safety data management in the pharmaceutical industry.

How does a MedDRA specialist typically collaborate with clinical and regulatory teams during the drug development process?

A MedDRA specialist plays a crucial role in ensuring accurate medical coding of adverse events and medical histories in clinical trials. They work closely with clinical research associates, data managers, and regulatory affairs professionals to standardize terminology and ensure compliance with regulatory requirements. Regular communication and collaboration are essential, as MedDRA specialists often provide guidance on coding conventions, review data for consistency, and help resolve complex coding queries. This cross-functional teamwork helps maintain data quality and supports timely regulatory submissions.

What is MedDRA?

MedDRA, which stands for Medical Dictionary for Regulatory Activities, is a standardized medical terminology system used globally to categorize and code medical information related to pharmaceuticals, such as adverse event reports, clinical trial data, and regulatory submissions. It helps ensure consistency and accuracy in how medical data is reported and analyzed across different countries and organizations. MedDRA is widely used by regulatory authorities, the pharmaceutical industry, and clinical research organizations to improve communication and safety monitoring in healthcare.

What is the difference between Meddra vs Medical Coder?

AspectMeddraMedical Coder
Required CredentialsTypically requires clinical terminology knowledge, coding experience, and sometimes certification in medical coding or terminologyRequires certification such as CPC, CCS, or CCS-P, with knowledge of medical coding standards
Work EnvironmentOften in healthcare settings, research, or pharmacovigilancePrimarily in hospitals, clinics, insurance companies, or coding service providers
Employer & Industry UsageUsed mainly in healthcare research, pharmacovigilance, and clinical data analysisUsed across healthcare providers, insurance companies, and coding agencies
Common Search & Comparison IntentUnderstanding differences in medical terminology coding systemsClarifying 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.

More about Meddra jobs

What cities are hiring for Meddra jobs?

Cities with the most Meddra job openings:

What states have the most Meddra jobs?

States with the most job openings for Meddra jobs include:

Infographic showing various Meddra job openings in the United States as of August 2026, with employment types broken down into 23% Full Time, 76% Part Time, and 1% Contract. Highlights an 18% Physical, 1% Hybrid, and 81% Remote job distribution, with an average salary of $53,009 per year, or $25.5 per hour.

GPV Functional QA Sr. Consultant

Deloitte

Princeton, NJ • On-site

Full-time

Re-posted 9 days ago


Deloitte rating

8.2

Company rating: 8.2 out of 10

Based on 92 frontline employees who took The Breakroom Quiz

44th of 150 rated financial services


Job description

Are you an experienced, passionate pioneer in technology who wants to work in a collaborative environment? As an experienced Global Pharmacovigilance Functional QA Senior Consultant you will have the ability to share new ideas and collaborate on projects as a consultant without the extensive demands of travel. If so, consider an opportunity with Deloitte under our Project Talent Model. Project Talent Model (PTM) is a talent model that is tailored specifically for long-term, onsite client service delivery.
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
The Team
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
The wage range for this role takes into account the wide range of factors that are considered in making compensation decisions including but not limited to skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Deloitte, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current range is $120,200 - $145,000.
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.
Recruiting tips
From developing a stand out resume to putting your best foot forward in the interview, we want you to feel prepared and confident as you explore opportunities at Deloitte. Check out recruiting tips from Deloitte recruiters.
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
Deloitte's purpose is to make an impact that matters for our people, clients, and communities. At Deloitte, purpose is synonymous with how we work every day. It defines who we are. Our purpose comes through in our work with clients that enables impact and value in their organizations, as well as through our own investments, commitments, and actions across areas that help drive positive outcomes for our communities. Learn more.
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

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