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Senior Clinical Terminology Jobs in Raleigh, NC (NOW HIRING)

Veranex

Sr Clinical Research Associate

Raleigh, NC · On-site

$98K - $140K/yr

The Sr. CRA will participate in the planning, development, and execution of clinical trials to ... Familiarity with medical and anatomical terminology. * Ability and willingness to travel Preferred ...

MMS

Senior Biostatistician - Remote (US)

Raleigh, NC · On-site

Senior Biostatistician: Responsibilities: * Create randomization and kit schedules independently ... Basic understanding of CROs and scientific & clinical data/terminology, & the drug development ...

Select Source International

Case Manager

Durham, NC · On-site

$19.25 - $25/hr

Minimum of 3 years full time direct clinical experience in an acute medical or acute surgical ... FEP and Senior Segment: Certified Case Manager (CCM) certification is required within 3 years of ...

Select Source International

Case Manager

Durham, NC · On-site

$19.25 - $25/hr

Minimum of 3 years full time direct clinical experience in an acute medical or acute surgical ... FEP and Senior Segment: Certified Case Manager (CCM) certification is required within 3 years of ...

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Senior Clinical Terminology information

See Raleigh, NC salary details

$21.4K

$121.8K

$200.2K

How much do senior clinical terminology jobs pay per year?

As of Aug 27, 2026, the average yearly pay for senior clinical terminology in Raleigh, NC is $121,792.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,600.00 and $152,600.00 per year, depending on experience, location, and employer.

What is the difference between Senior Clinical Terminology vs Clinical Data Analyst?

AspectSenior Clinical TerminologyClinical Data Analyst
CredentialsTypically requires certifications in clinical terminology systems (e.g., SNOMED CT, LOINC)Often holds degrees in health informatics, data analysis, or related fields; may also have certifications in data analysis tools
Work EnvironmentWorks within healthcare organizations, focusing on coding, terminology management, and clinical data standardizationWorks in research, healthcare, or pharmaceutical companies analyzing clinical data sets and generating reports
Employer & Industry UsageCommonly employed in hospitals, EHR vendors, and health IT companiesFound in research institutions, healthcare providers, and pharmaceutical companies

While both roles involve working with clinical data, Senior Clinical Terminology specialists focus on managing and standardizing clinical vocabularies, whereas Clinical Data Analysts analyze data to support research and decision-making. Understanding these differences helps in choosing the right career path or job search focus.

What does a senior clinical terminology do?

A senior clinical terminology specialist manages and maintains standardized medical vocabularies and coding systems, such as SNOMED CT or LOINC, to ensure accurate clinical data representation. They often collaborate with healthcare IT teams, review terminology updates, and may use tools like terminology management software to support clinical documentation and data exchange.

What are popular job titles related to Senior Clinical Terminology jobs in Raleigh, NC?

For Senior Clinical Terminology jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Senior Clinical Terminology jobs in Raleigh, NC look for?

The top searched job categories for Senior Clinical Terminology jobs in Raleigh, NC are:

Senior Clinical Terminology jobs near you
Infographic showing various Senior Clinical Terminology job openings in Raleigh, NC as of August 2026, with employment types broken down into 2% As Needed, 78% Full Time, 13% Part Time, and 7% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $121,792 per year, or $58.6 per hour.

Sr Clinical Research Associate

Raleigh, NC • On-site

Veranex
Medical Equipment and Supplies Manufacturing • 501 - 1,000 employees
Learn more about Veranexexternal

$98K - $140K/yr

Other

Re-posted 14 days ago

Job description

Veranex's mission as an Innovation CRO is to improve patient outcomes by accelerating our clients' innovations to market. As the world's only end-to-end professional services firm focused on MedTech, we take clients' Vision to Velocity through our comprehensive service portfolio, with expertise in human centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting.
The Veranex Clinical Operations team is a dynamic group of professionals providing regulatory, quality and clinical services for the medical device industry. Our team supports start-ups, mid-sized private companies, and the largest corporations at all stages of the product life cycle. We work across a broad spectrum of technologies and treatment modalities. Our clients develop both next-generation and paradigm-shifting devices. Our product exposure includes implantables, instruments (manual, laser, robotic, etc.), capital equipment, combination products, software as a medical device (SaMD), medical mobile apps, in vitro diagnostics and more
About This Role:
Veranex has an exciting opportunity to join our team as a Senior Clinical Research Associate to support our Clinical Operations team. The Sr. CRA will participate in the planning, development, and execution of clinical trials to evaluate the safety, effectiveness and performance of medical devices. Under management supervision, the Sr. CRA will monitor assigned clinical trials to ensure adherence to the clinical protocol, applicable regulations, and company Standard Operating Procedures (SOPs) governing clinical studies.
Location: Remote, US
What You Will Do:
  • Responsible for ensuring that study investigators and coordinators comply with the study protocol, Good Clinical Practices (GCPs), Code of Federal Regulations (CFRs), and Institutional Review Board (IRB)/Ethics Committee (EC) requirements during clinical studies by training/guidance of investigators/research coordinators, conducting periodic on-site evaluations and follow-up of corrective actions
  • Acts as primary liaison to clinical sites.
  • Conducts site qualification visits, study start-up activities (essential document collection), site qualification visits, site initiation visits and training, monitoring visits for source data verification (reported study data are accurate, complete, and verifiable from source documents in the site's medical records), and site close-out visits. Generates high-quality site qualification, initiation, monitoring, and close-out visit reports in timely manner (in accordance with the Clinical Monitoring Plan)
  • Contributes to protocol, informed consent, case report form (CRF) and study plan development as well as annual progress reports (APRs) and the clinical study report (CSR) at study conclusion to report the study results to FDA and other regulatory authorities
  • Ensures that the rights and well-being of human subjects are protected and confirms data quality/integrity by maintaining site compliance, reviewing adverse events and device deficiencies, reviewing data trending/metrics, reviewing audit reports, and implementing corrective actions as necessary
  • Supports maintenance of department SOPs and work instructions
  • Supports investigational device traceability including documentation for forecasting, shipping, receipt, and disposition.
  • Supports and maintains documentation of all clinical research activities in the study trial master file (TMF), e.g., monitoring reports, site correspondence, device inventory information.
  • Drives trial enrollment and identifies and communications potential and actual obstacles to enrollment.
  • Travel requirement: 25-50%

Qualifications:
Required skills:
  • Minimum of 5 years of directly related work experience or equivalent in clinical research, including work on medical device significant risk IDE trials and/or non-significant risk abbreviated IDE trials.
  • Must be able to work autonomously and as a member of a cross-functional team and meet high expectations and tight deadlines. May work on highly visible projects in high-pressure situations
  • Must have working knowledge of Good Clinical Practices (GCPs), FDA regulations and IRB requirements.
  • Must have strong project management competencies and ability to work with high quality, reliability, and attention to detail.
  • Must have a strong level of professionalism, including verbal and written communication skills; and the ability to communicate with all levels of the organization, cross-functionally, and with clients/partners.
  • Must have proficiency in using Microsoft Office Suite, including Word, Excel, Outlook and PowerPoint; as well as experience with electronic data capture (EDC) and electronic Trial Master File (eTMF) systems.
  • Experience interfacing successfully with physicians/clinical staff and familiarity with hospital/clinical environments
  • Familiarity with medical and anatomical terminology.
  • Ability and willingness to travel

Preferred:
  • BS or BA degree preferred; BS or BA in a relevant scientific discipline or related field also preferred.

Veranex is an equal opportunity employer and prohibits discrimination of any kind. All qualified applicants will receive consideration for employment without regard for race, color, religion or belief, sex (including pregnancy, gender identity or gender expression), sexual orientation, parental or marital status, disability, age, status as a protected veteran, national, social, or ethnic origin, or any other applicable legally protected characteristics.

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