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Meddra Coding Jobs in Massachusetts (NOW HIRING)

Medical Coder

Cambridge, MA

$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 ...

Director, Safety Scientist

Boston, MA · On-site

$175K - $263K/yr

Experience in MedDRA coding and search strategies * Excellent, independent judgment based on knowledge and expertise * Strong personal time-management and project-management skills * Mastery of ...

Experience in MedDRA coding and search strategies * Excellent, independent judgment based on knowledge and expertise * Strong personal time-management and project-management skills * Mastery of ...

Showing results 21-40

Meddra Coding information

See Massachusetts salary details

$9

$21

$32

How much do meddra coding jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for meddra coding in Massachusetts is $21.02, according to ZipRecruiter salary data. Most workers in this role earn between $12.36 and $29.13 per hour, depending on experience, location, and employer.

How do I get trained in Meddra coding?

Training for MedDRA coding typically involves completing specialized courses offered by organizations such as the Uppsala Monitoring Centre or through online platforms. These courses cover terminology, coding guidelines, and software tools, and often require prior knowledge of pharmacovigilance or medical terminology.

What is a MedDRA coding?

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, individuals typically complete relevant training in medical coding and gain experience in clinical documentation. Certification is often achieved through specialized programs or courses offered by industry organizations, and proficiency in coding tools and terminology is essential.

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, familiarity with medical concepts and use of coding tools can facilitate learning over time.
What cities in Massachusetts are hiring for Meddra Coding jobs? Cities in Massachusetts with the most Meddra Coding job openings:
Infographic showing various Meddra Coding job openings in Massachusetts as of August 2026, with employment types broken down into 88% Full Time, 6% Part Time, and 6% Contract. Highlights an 77% In-person, 6% Hybrid, and 17% Remote job distribution, with an average salary of $43,723 per year, or $21 per hour.

Associate Director, Safety Scientist Boston, Massachusetts, United States of America LGY_CDSU -[...]

Alexion Pharma Spain S.L.

Boston, MA • On-site

$126 - $190/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 3 days ago

New


Job description

## Associate Director, Safety ScientistBoston, Massachusetts, United States of AmericaApply NowFind out how well you match with this jobThe Associate Director, Safety Scientist plays a leadership role within Global Patient Safety (GPS) to actively evaluate and manage risk in collaboration with the GPS Medical Director(s) and cross-functional team members within the global regulatory framework.**You will be responsible for:*** Managing safety scientist activities across multiple product portfolios and/or indications* Organizing, training and/or supporting junior safety scientists and fellows* Supporting activities related to new drug applications and other regulatory filings* Representing global patient safety at regulatory inspections e.g., MHRA, FDA, EMA, etc.* Leading gap analysis to ensure alignment with changes in global regulations* Strategizing and drafting of responses to regulatory inquiries on product safety issues inclusive of defining MedDRA search strategy* Representing GPS in global program teams and associated cross functional teams and/or projects as needed* Proactively providing guidance and educational training to GPS therapeutic teams* Responsible for Signal Review Meeting and Signal Management Team activities in collaboration with GPS Medical Directors* Performing Signal Surveillance activities for respective programs in collaboration with GPS Medical Directors* Project managing and authoring of safety documents including PSUR, PBER, PADER, RMP, REMS, CSRs, and ad hoc requests in collaboration with GPS Medical Directors* Authoring safety sections, in collaboration with team members, on regulatory responses, IBs/CCDS, protocols, ICFs, Data Monitoring Committee reports and requests, and other documents, and provide the necessary quality control to ensure alignment with core safety position.* Manage portfolio of products/projects related to risk management; assists GPS Medical Directors in the development of risk management strategy and activities for assigned products* Contribute to on-going process enhancement for safety analytics and reporting, such as developing standard procedures and templates* Assisting GPS Medical Directors to oversee risk minimization activities including tracking of activities as needed* May be directed by the line function to support initiatives outside of their projects**You must have:*** Bachelor's degree in a biologic/medical/clinical/nursing field* At least 5 years' experience in drug safety and risk management within the pharmaceutical, biotech or CRO industry* Knowledge and understanding of US and EU safety regulations pre- and post- marketing* Experience with Risk Management and Minimization programs* Experience preparing post marketing safety regulatory documents including PSURs, PBRERs and Risk Management Plans* Experience with clinical development including risk/benefit analysis and safety assessment* Strong clinical, analytical, problem solving and scientific writing and communication skills* Ability to interact effectively with people of multiple disciplines and cultures both within and outside the company on a global basis* Expertise with Microsoft Word, PowerPoint, SharePoint and Excel**Nice to have:*** Advanced degree in a biologic/medical/clinical/nursing field preferred: Pharmacist/PharmD, Nurse Practitioner or PhD* Expertise with clinical and safety databases* Experience in MedDRA coding and search strategies* Excellent, independent judgment based on knowledge and expertise* Strong personal time-management and project-management skills* Knowledge of Power BI, and other visualization tools*The annual base pay ranges from $126,000 to $190,000. Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.***Date Posted**16-Jul-2026**Closing Date**31-Jul-2026Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form. #J-18808-Ljbffr