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From Home Meddra Coding Jobs (NOW HIRING)

JenaValve

Specialist, Clinical Safety

Irvine, CA · On-site

$100K/yr

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.

Integrated Resources INC

Drug Safety

Horsham, PA

... from the LSO or Call Centre Discuss source documents, coding conventions and ad-hoc queries with ... Standard Operating Procedures and Working Practices Department guidance documents MedDRA coding ...

Exelixis

Drug Safety Associate II - Study Ops

Alameda, CA · On-site

$116K - $165K/yr

Processing and assessing SAEs from receipt at Exelixis to case closure in the Argus database, including query generation, narrative and ASE writing. * MedDRA coding of SAEs and AEs as reported in ...

Exelixis

Drug Safety Associate II - Study Ops

Alameda, CA · On-site

$116K - $165K/yr

Processing and assessing SAEs from receipt at Exelixis to case closure in the Argus database, including query generation, narrative and ASE writing. * MedDRA coding of SAEs and AEs as reported in ...

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How much do from home meddra coding jobs pay per hour?

As of Jun 29, 2026, the average hourly pay for from home meddra coding in the United States is $19.25, according to ZipRecruiter salary data. Most workers in this role earn between $11.30 and $26.68 per hour, depending on experience, location, and employer.

Can you work from home being a medical coder?

Medical coders, including those specializing in MedDRA coding, often have the option to work from home, especially with the increasing use of electronic health records and coding software. Remote work typically requires strong computer skills, attention to detail, and relevant certifications such as CPC or CCS, along with reliable internet access. However, some employers may require in-office presence for training or quality assurance purposes.

What is the difference between From Home Meddra Coding vs From Home Medical Coder?

AspectFrom Home Meddra CodingFrom Home Medical Coder
CertificationsMedDRA coding certification, medical terminology knowledgeAHIMA or AAPC coding certification, medical terminology knowledge
Work EnvironmentRemote, healthcare data analysisRemote, medical record review and coding
Industry UsagePharmaceuticals, clinical researchHospitals, clinics, insurance companies
Search & Comparison IntentUnderstanding MedDRA coding rolesMedical coding for billing and records

From Home Meddra Coding involves assigning standardized medical terminology to clinical data, primarily for research and regulatory purposes. From Home Medical Coder focuses on translating medical records into billing codes for healthcare reimbursement. While both roles require medical terminology knowledge and remote work skills, they serve different industry needs and use different certifications.

How to become a certified MedDRA coder?

To become a certified MedDRA coder, individuals typically complete specialized training in MedDRA coding, gain experience in medical coding or pharmacovigilance, and pass certification exams offered by organizations such as the MSSO (Medical Dictionary for Regulatory Activities Maintenance and Support Organization). Proficiency in medical terminology, coding tools, and regulatory guidelines is essential for certification and effective job performance.

Is AI replacing medical coders?

AI is increasingly used to assist medical coders by automating routine coding tasks and improving accuracy, but it does not fully replace human coders. Medical coders, including those specializing in from home Meddra coding, are still essential for complex cases, quality assurance, and interpreting nuanced clinical information. Human oversight remains critical to ensure compliance and accuracy in medical coding processes.

How much do medical billers and coders make working from home?

Medical billers and coders working from home typically earn between $15 and $30 per hour, with annual salaries ranging from approximately $30,000 to $65,000 depending on experience, certifications, and location. Many remote positions require proficiency in coding software and industry standards like ICD-10 and CPT codes.

What are the key skills and qualifications needed to thrive as a From Home MedDRA Coder, and why are they important?

To excel as a From Home MedDRA Coder, you need a solid understanding of medical terminology, pharmacovigilance principles, and experience with MedDRA coding, often supported by a degree in life sciences or a related field. Familiarity with safety databases, coding software, and regulatory reporting systems such as Argus or Oracle is typically required. Attention to detail, analytical thinking, and strong written communication are crucial soft skills for ensuring accurate and consistent coding. These competencies are vital to maintain data quality and compliance with regulatory standards in remote pharmacovigilance operations.

What are some common challenges faced by professionals working from home as MedDRA coders, and how can these be managed?

Working from home as a MedDRA coder offers flexibility but also presents challenges such as maintaining focus, managing communication with clinical teams, and keeping up with regulatory updates. To address these, it's important to establish a structured work routine, utilize secure and efficient communication tools, and participate in regular virtual meetings or training sessions. Staying organized and proactive about continuing education helps ensure accuracy in coding and compliance with industry standards.
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From Home Meddra Coding jobs near you
Specialist, Clinical Safety

Specialist, Clinical Safety

JenaValve

Irvine, CA • On-site

$100K/yr

Full-time

Posted yesterday

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