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Remote Meddra Coding Jobs (NOW HIRING)

Talent Software Services

Sr. Medical Writer

California, MO · Remote

$70 - $80/hr

Talent Software Services is in search of a Sr. Medical Writer for a contract position in CA (Remote ... of coding dictionaries (MedDRA, WHO Drug)Computer/office equipment SkillsProficient in Microsoft ...

Emmes

Medical Officer

Rockville, MD · Remote

Reviews and approves Medical Dictionary for Regulatory Activities (MedDRA) and WHO Drug coding ... Remote Employment Type: FULL_TIME

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How much do remote meddra coding jobs pay per hour?

As of Jun 3, 2026, the average hourly pay for remote meddra coding in the United States is $21.50, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $22.84 per hour, depending on experience, location, and employer.

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

To thrive as a Remote MedDRA Coder, you need a strong background in life sciences or healthcare, familiarity with medical terminology, and experience in pharmacovigilance or clinical data management. Proficiency with MedDRA coding software, safety databases (such as Argus or Oracle), and relevant certifications like MedDRA training are commonly required. Attention to detail, analytical thinking, and effective written communication help ensure accurate and consistent medical coding. These skills and qualifications are essential for maintaining data quality, regulatory compliance, and supporting patient safety in clinical research and drug safety reporting.

What are some common challenges faced by professionals in remote MedDRA coding roles, and how can they be addressed?

Remote MedDRA coders often face challenges such as maintaining data consistency across different projects, staying updated with regular MedDRA version changes, and effectively communicating with global pharmacovigilance or clinical teams. To address these, it's important to follow established coding guidelines, participate in ongoing training, and use collaboration tools for regular check-ins with team members. Proactively seeking clarification and documenting coding decisions can also help ensure accuracy and support team alignment.

What is remote MedDRA coding?

Remote MedDRA coding involves assigning standardized medical terminology codes from the MedDRA (Medical Dictionary for Regulatory Activities) system to medical information, such as adverse event reports, from a remote location. This process helps ensure consistency and accuracy in the reporting of medical data for regulatory submissions and pharmacovigilance. Remote MedDRA coders typically work for pharmaceutical companies, CROs, or regulatory agencies, reviewing clinical data and using specialized software to code terms according to MedDRA guidelines.

What is the difference between Remote Meddra Coding vs Remote Medical Coding?

AspectRemote Meddra CodingRemote Medical Coding
CertificationsMedDRA certification, coding credentialsAHIMA or AAPC medical coding certifications
Work EnvironmentRemote, healthcare, pharmaceutical, or clinical research settingsRemote, healthcare facilities, insurance companies, or billing services
Industry UsagePharmaceuticals, clinical trials, regulatory agenciesHospitals, clinics, insurance companies, billing companies
Search & Comparison IntentUnderstanding specialized coding for drug safety and regulatory purposesGeneral medical billing and coding for healthcare providers

Remote Meddra Coding focuses on coding for drug safety and regulatory submissions using MedDRA standards, often in pharmaceutical or clinical research contexts. Remote Medical Coding covers a broader range of medical billing and coding tasks for healthcare providers. While both roles require coding certifications, their industry applications and work environments differ, making each role specialized for distinct healthcare and regulatory needs.

More about Remote Meddra Coding jobs
What cities are hiring for Remote Meddra Coding jobs? Cities with the most Remote Meddra Coding job openings:
What are the most commonly searched types of Meddra Coding jobs? The most popular types of Meddra Coding jobs are:
What states have the most Remote Meddra Coding jobs? States with the most job openings for Remote Meddra Coding jobs include:
What job categories do people searching Remote Meddra Coding jobs look for? The top searched job categories for Remote Meddra Coding jobs are:
Remote Meddra Coding jobs near you
Infographic showing various Remote Meddra Coding job openings in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $44,724 per year, or $21.5 per hour.
Director, Data Systems and Clinical Programming

Director, Data Systems and Clinical Programming

Alumis

South San Francisco, CA • On-site, Remote

$200K - $225K/yr

Other

Posted 14 days ago

Job description

The Director, Data Systems (DS) and Clinical Programming (CP) will be responsible for leading and managing the Clinical Programming function within Data Management (DM). This position will report to the VP, Data Management and Clinical Programming.

Responsibilities: 
  • Lead and manage the Data Systems and Clinical Programming function within DM
  • Drive the implementation of various technology solutions to augment existing DM processes, optimize efficiency and enhance overall data quality assurance
  • Lead and/or participate in AI-related initiatives for DM
  • Develop and implement strategies for optimizing data flow, database builds, and integration of external technologies.
  • Oversee the validation of the EDC platform, ensuring ongoing system optimization.
  • Manage relationships with key external vendors, ensuring alignment with organizational goals.
  • Ensure compliance with all relevant data privacy regulations and maintain the security of clinical trial data.
  • Ensure DS&CP project deliverables are completed on time and in accordance with quality standards and regulatory requirements.
  • Collaborate with other departments to align data strategy with broader organizational goals and objectives.
  • Mentor and develop team members, fostering a culture of continuous learning and growth within the team.
  • Oversee all SAS clinical programming requests and standardize the clinical programming specification development process.
  • Develop and/or maintain Alumis' standard CRFs and standard edit checks, inclusive of indication-specific standards.
  • Develop DS&CP SOPs and Work Instructions.
  • Lead the development and/or maintenance of standard vendor Data Transfer Agreements (DTAs).
  • Oversee the development and execution of technical initiatives within DM, including the implementation of key data visualizations and dashboards for DM, such as Clean Patient Tracking, data currency, and rolling batch freeze progress.
  • Integrate the usage of data analytics within DM to further optimize current processes.
  • Provide strategic oversight of high-priority projects, including database builds, user access management, and the release of system updates.
  • Participate in EDC, IRT and eCOA User Acceptance Testing (UAT)
  • Ensure accurate development and execution of data integrations between EDC, IXRS or additional external vendor data sources
  • Ensure DS&CP study-specific documentation is in an inspection-ready state and represent the DS&CP function in inspections as applicable.
  • Represent DS&CP in cross-functional meetings as applicable
  • Act as a key stakeholder in developing and executing strategies to accelerate drug development through innovative data management practices.
Qualifications: 
  • 12+ years of relevant experience and has earned a BS or equivalent degree; MS or MBA a plus
  • Experience supporting Ph I-IV clinical trials, both in-house and through CRO partners
  • Strong knowledge and experience in EDC and other key technologies (e.g., IXRS, data visualization) 
  • Proficiency in CDISC standards (CDASH, SDTM, ADaM)
  • Experience with SAS, SQL and/or other clinical programming tools
  • Proficiency in clinical research regulations and guidance, including FDA CFR and ICH GCP 
  • Depth of experience across all aspects of DM, including but not limited to: CRF and database development, data quality assurance and analytics, data transfer management, vendor management, DM study documentation and inspection readiness. 
  • Strong understanding of the application of MedDRA and WHO Drug clinical data coding classification systems
  • Strong interpersonal, organizational, and communication (oral and written) skills
  • Demonstrated ability to cultivate strong working relationships with internal and external colleagues.
  • Logical thinking, attention to detail and accuracy, strong organizational skills, and problem-solving abilities
  • Ability to prioritize and to adapt quickly to changing business conditions with a "can-do" attitude
  • Capable of proactively identifying project challenges and risks and proposing appropriate and strategic solutions to issues.
  • Willing to travel if required  

Alumis Values 
We Elevate 
We Challenge 
We Nurture 

This position is located in South San Francisco, CA and employees are expected to be onsite Tuesday-Thursday. Open to remote applicants with requirement to be onsite 1-2x a quarter.

The salary range for this position is $200,000 USD to $225,000 USD annually. This salary range is an estimate, and the actual salary may vary based on the Company's compensation practices.

Alumis Inc. is an equal opportunity employer.

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