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Meddra Jobs (NOW HIRING)

TechData Service Company LLC

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Medical Writer (Remote)

OR · Remote

$85 - $90/hr

Familiarity with medical terminology and coding dictionaries such as MedDRA and WHODrug. Strong knowledge of ICH/GCP and regulatory submission requirements. Epilepsy or neurology experience is a plus.

Artivion

Sr. Clinical Data Manager

Kennesaw, GA

Conduct and oversee data reconciliation, external data integrations (labs, imaging, etc.), and coding of medical terms (MedDRA, WHO-DD). * Provide study specific reports and data listings on regular ...

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How much do meddra jobs pay per hour?

As of Jul 1, 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, and why are they important?

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 and what is it used for?

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:
What job categories do people searching Meddra jobs look for? The top searched job categories for Meddra jobs are:
Meddra jobs near you
Infographic showing various Meddra job openings in the United States as of June 2026, with employment types broken down into 97% Full Time, and 3% Contract. Highlights an 69% Physical, 5% Hybrid, and 26% Remote job distribution, with an average salary of $53,009 per year, or $25.5 per hour.
Medical Writer (Remote)

Medical Writer (Remote)

TechData Service Company LLC

OR • Remote

$85 - $90/hr

Contractor

Medical, Dental

Posted 3 days ago

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Key responsibilities

  • Author, review, and edit clinical and regulatory documents, including protocols, clinical study reports, investigator's brochures, informed consent forms, CTD clinical modules, briefing documents, safety reports, and responses to regulatory questions.

  • Collaborate with cross-functional teams and external vendors to manage document timelines, review cycles, and submission-ready deliverables.

  • Ensure documents comply with ICH, GCP, FDA, EMA, and other applicable regulatory guidelines.

Job description

Company: Biotechnology Company

Title: Medical Writer

Contract Position - 6 months with potential extension

Position Summary
Our client is seeking an experienced Medical Writer to develop high-quality clinical and regulatory documents in support of clinical development and regulatory submissions. This role will partner with Clinical Development, Regulatory Affairs, Biostatistics, Medical Affairs, Quality Assurance, and external vendors to produce clear, accurate, and compliant documents.
Key Responsibilities
Author, review, and edit clinical and regulatory documents, including protocols, protocol amendments, clinical study reports, investigator’s brochures, informed consent forms, CTD clinical modules, briefing documents, safety reports, and responses to regulatory questions.
Support clinical development activities by helping prepare clinical development plans, protocols, and related study documents.
Interpret complex clinical and scientific data and communicate findings clearly and accurately.
Ensure documents comply with ICH, GCP, FDA, EMA, and other applicable regulatory guidelines.
Collaborate with cross-functional teams to manage document timelines, review cycles, and submission-ready deliverables.
Review documents prepared by internal teams or external vendors for clarity, consistency, scientific accuracy, and regulatory compliance.
Qualifications
Advanced degree preferred, such as PhD, PharmD, MD, or MSc in Life Sciences, Medicine, Pharmacy, or a related field.
Minimum 3–5 years of medical writing experience in the pharmaceutical, biotech, or CRO industry.
Strong experience writing clinical trial and regulatory submission documents.
Knowledge of drug development, clinical research, clinical study conduct, regulatory requirements, and biostatistical concepts.
Familiarity with medical terminology and coding dictionaries such as MedDRA and WHODrug.
Strong knowledge of ICH/GCP and regulatory submission requirements.
Epilepsy or neurology experience is a plus.
Veeva experience preferred.
Proficiency with Microsoft Word, Excel, PowerPoint, Adobe Acrobat, EndNote, and document management systems.
Ideal Candidate
The ideal candidate is a detail-oriented medical writer who can manage multiple projects, work independently, collaborate effectively with cross-functional teams, and produce clear, well-structured, submission-ready clinical and regulatory documents.

Company Description

www.techdataservice.com