Apply knowledge of medical coding systems (e.g., ICD-10, MedDRA, CPT, HCPCS) and standard of care guidelines, to interpret, classify and categorize abstracted clinical data points from unstructured ...
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Apply knowledge of medical coding systems (e.g., ICD-10, MedDRA, CPT, HCPCS) and standard of care guidelines, to interpret, classify and categorize abstracted clinical data points from unstructured ...
Meddra Coding information
See Texas salary details
$8.51 - $10.26
21% of jobs
$10.63 is the 25th percentile. Wages below this are outliers.
$10.26 - $12.01
20% of jobs
$12.01 - $13.76
8% of jobs
The median wage is $14.11 / hr.
$13.76 - $15.51
5% of jobs
$15.51 - $17.26
0% of jobs
$17.26 - $19.02
0% of jobs
$19.02 - $20.77
0% of jobs
$20.77 - $22.52
9% of jobs
$24.27 is the 75th percentile. Wages above this are outliers.
$22.52 - $24.27
11% of jobs
$24.27 - $26.02
13% of jobs
$26.02 - $27.77
13% of jobs
$8
$17
$27
How much do meddra coding jobs pay per hour?
As of Jun 15, 2026, the average hourly pay for meddra coding in Texas is $17.93, according to ZipRecruiter salary data. Most workers in this role earn between $10.53 and $24.86 per hour, depending on experience, location, and employer.
How do I get trained in MedDRA coding?
Training in MedDRA coding typically involves completing specialized courses offered by the MedDRA Maintenance and Support Services Organization (MSSO) or accredited training providers. These courses cover terminology, coding rules, and software tools, and often lead to certification that demonstrates proficiency in MedDRA coding standards.
What is the highest paid medical coder job?
Senior or specialized medical coders, such as those with credentials like Certified Professional Coder (CPC) or Certified Coding Specialist (CCS), tend to earn the highest salaries in medical coding. Positions involving coding for complex specialties like radiology, cardiology, or oncology often offer higher pay, especially with experience and advanced certifications.
What is a MedDRA Coding job?
A MedDRA Coding job involves assigning standardized Medical Dictionary for Regulatory Activities (MedDRA) terms to adverse events, medical conditions, and drug-related data in clinical trials and pharmacovigilance. Coders ensure consistency and accuracy in medical terminology to support regulatory reporting and safety analysis. This role requires knowledge of MedDRA hierarchy, coding guidelines, and industry regulations. Professionals often work in pharmaceutical companies, contract research organizations (CROs), or regulatory agencies. Strong attention to detail and familiarity with medical terminology are essential skills for this job.
How to become a certified MedDRA coder?
To become a certified MedDRA coder, professionals typically complete training programs offered by the MedDRA Maintenance and Support Services Organization (MSSO) or authorized training providers, gaining knowledge of coding principles and terminology. Certification is often achieved through passing assessments that demonstrate proficiency in MedDRA coding, which may be required by employers in pharmacovigilance, clinical research, or regulatory roles.
What are the key skills and qualifications needed to thrive in the Meddra Coding position, and why are they important?
To excel in MedDRA Coding, a strong understanding of medical terminology, clinical research processes, and pharmacovigilance concepts—often supported by a life sciences degree or healthcare background—is essential. Familiarity with the MedDRA (Medical Dictionary for Regulatory Activities) system, coding software, and relevant regulatory guidelines, along with certifications in drug safety or medical coding, is highly valued. Attention to detail, analytical thinking, and effective communication are standout soft skills for this position. These competencies are crucial to ensure accurate and consistent coding of medical terms, enabling high-quality safety data analysis and regulatory compliance.
What are the typical responsibilities of a MedDRA Coding specialist on a clinical research or pharmacovigilance team?
A MedDRA Coding specialist is primarily responsible for translating medical information from clinical trial reports, adverse event forms, or safety databases into standardized MedDRA terms. This ensures accurate data capture, analysis, and reporting for regulatory submissions and ongoing safety monitoring. Specialists often collaborate with drug safety teams, medical writers, and data managers to resolve coding discrepancies and maintain consistency in terminology. In addition, the role may involve participating in cross-functional meetings and providing coding support during audits or inspections. Working efficiently and maintaining up-to-date knowledge of MedDRA updates are also key aspects of the job.
Is MedDRA coding difficult to learn?
MedDRA coding for medical coding professionals involves understanding complex medical terminology and classification systems, which can require dedicated training and practice. While some find it challenging initially, proficiency improves with experience, and many organizations offer training programs or certifications to facilitate learning.
What are popular job titles related to Meddra Coding jobs in Texas? For Meddra Coding jobs in Texas, the most frequently searched job titles are:
What job categories do people searching Meddra Coding jobs in Texas look for? The top searched job categories for Meddra Coding jobs in Texas are:
Full-time
Medical, Dental, Vision, Life, Retirement
Posted 25 days ago
Natera rating
7.7
Based on 35 frontline employees who took The Breakroom Quiz
47th of 103 rated laboratories
Job description
POSITION SUMMARY:
Perform high-quality medical record abstraction by combining proficient-level experiences in data management and software with medical terminology, medical coding, information encoding, and analytical capabilities. Interpret and manage complex clinical patient data for research, quality improvement, and regulatory reporting.
PRIMARY RESPONSIBILITIES:
Data Abstraction: Accurately review, interpret, and abstract clinical patient data from various electronic health record (EHR) systems, paper charts, and other source documents in accordance with defined project or research protocols, clinical, data, and technical specifications, and dictionaries.
Coding and Classification: Apply knowledge of medical coding systems (e.g., ICD-10, MedDRA, CPT, HCPCS) and standard of care guidelines, to interpret, classify and categorize abstracted clinical data points from unstructured text to standardized machine readable data in one common database schema.
Electronic Data Capture (EDC): Utilize specialized data management software (e.g., REDCap, registries, and custom built EDC systems) to enter, track, and maintain the integrity of clinical data encoded into queryable databases.
Technical Support: Aid cross-functional teams in translating clinical and data abstraction and encoding requirements. Support prompt engineering and design for all AI and LLM initiatives.
Data Management: Apply and support establishing program specific clinical data management best practices (CGDMP) and good clinical practice (GCP) during the abstraction and encoding process resulting in accurate, legible, contemporaneous, original, attributable, complete and consistent for end-to-end ETL workflows.
Quality Assurance and Control: Apply industry standard best practices for utilizing real-world data for research, quality monitoring, and regulatory reporting using technical and analytical software such as running MACROs and using Excel/Google Sheets functions and formulas, and pivot tables to support ensuring abstracted data are accurate and clinical complete.
Mentoring and Subject Matter Expertise (SME): Conduct peer reviews on medical record data interpreted and encoded by abstraction peers to ensure quality and productivity performance align with the programs expectations.
Protocol Adherence: Maintain strict adherence to all project and research protocols, institutional review board (IRB) requirements, HIPAA regulations, data management best practices (e.g., DAMA, SCDM, ACRP, and SOCRA), and organizational policies regarding patient privacy and data security.
Process Improvement: Participate in the development and refinement of abstraction and quality guidelines, tools, and standard operating procedures.
Daily Operations: Provide timely and accurate daily, weekly, or monthly abstraction submissions, productivity reporting, and actively participate in team meetings and workshops.
Certifications: Maintenance of all relevant clinical or technical licensures.
Other duties and responsibilities to be performed as assigned.
QUALIFICATIONS:
Clinical Background: U. S. licensed Nurse, PA-C, NP, or DNP is required with a Master's degree in health sciences. Strong understanding of medical terminology, disease processes (especially cancer), standard clinical workflows, and genetic testing.
Clinical Experience: Minimum of 4-5 years of experience in clinical data abstraction and medical records review, preferably in cancer, women's health, rare diseases.
Data Abstraction Expertise: Proven ability to accurately read, interpret, and abstract complex clinical information from various electronic and paper medical record sources.
Data Management Expertise: Direct experience performing clinical data encoding using standard ontologies including but not limited to ICD-10-CM and SNOMED CT. Direct experience performing data mapping, standardization, and harmonization.
Quality and Compliance: Demonstrated commitment to data integrity, quality control processes, and adherence to HIPAA and other data privacy regulations.
Technical Proficiency: Proficient with Microsoft Office Suite or Google Suite, creating pivot tables, generating reports, data analysis, and using clinical data systems or databases common in clinical data abstraction, research, or clinical data management (e.g., fillable forms, ECDs, data registries).
Certifications/Industry Expertise: CCDM, CCRP, ACR-P, or CRA preferred.
Communication: Excellent written and verbal communication skills, with the ability to effectively collaborate with clinical and non-clinical teams.
Autonomy: Proven ability to work independently, manage time effectively, prioritize and organize tasks, and meet strict productivity and quality deadlines.
General Expertise:
Possess a high level of initiative and self-motivation.
Capable of working part of a team on high visibility projects and tasks with high rates of communication.
In-depth attention to detail and a fast learner.
Responding to shifting priorities and changes.
OUR OPPORTUNITY
Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women's health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.
The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you'll work hard and grow quickly. Working alongside the elite of the industry, you'll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.
WHAT WE OFFER
Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!
For more information, visit www.natera.com.
Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.
All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.
If you are based in California, we encourage you to read this important information for California residents.
Link: https://www.natera.com/notice-of-data-collection-california-residents/
Please be advised that Natera will reach out to candidates with a @natera.com email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.
For more information:
- BBB announcement on job scams
- FBI Cyber Crime resource page