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Clinical Quality Specialist Rn Jobs in Raleigh, NC

TNAA TotalMed RN

Travel CVPICU RN

Durham, NC · On-site

You will collaborate with physicians, specialists and the patients' families to ensure the best ... clinicians of all specialties in all 50 states. They offer local and travel jobs and match ...

TNAA TotalMed RN

Travel CVPICU RN

Durham, NC · On-site

You will collaborate with physicians, specialists and the patients' families to ensure the best ... clinicians of all specialties in all 50 states. They offer local and travel jobs and match ...

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All JobsClinical Quality Specialist Rn JobsClinical Quality Specialist Rn Jobs in Raleigh, NC

Clinical Quality Specialist Rn information

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How much do clinical quality specialist rn jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for clinical quality specialist rn in Raleigh, NC is $41.46, according to ZipRecruiter salary data. Most workers in this role earn between $34.13 and $45.58 per hour, depending on experience, location, and employer.

What does a Clinical Quality Specialist RN do?

A Clinical Quality Specialist RN is a registered nurse who focuses on improving the quality and safety of patient care within healthcare organizations. Their responsibilities include analyzing clinical processes, monitoring compliance with regulatory standards, leading quality improvement initiatives, and educating staff on best practices. They collaborate with multidisciplinary teams to identify areas for improvement, implement evidence-based interventions, and track outcomes to ensure high standards of healthcare delivery. This role is essential in promoting patient safety and enhancing the overall effectiveness of healthcare services.

What are the key skills and qualifications needed to thrive as a Clinical Quality Specialist RN?

To thrive as a Clinical Quality Specialist RN, you need a robust clinical background, an active RN license, and expertise in quality improvement methodologies and healthcare regulations. Familiarity with data analysis tools, electronic health records (EHRs), and quality measurement systems like HEDIS or CMS guidelines is essential. Strong analytical thinking, attention to detail, and the ability to communicate complex information clearly are critical soft skills for this role. These competencies ensure that quality initiatives are effectively implemented, regulatory compliance is maintained, and patient care standards are continuously improved.

How does a Clinical Quality Specialist RN typically collaborate with clinical staff to improve patient care processes?

A Clinical Quality Specialist RN works closely with nurses, physicians, and other healthcare professionals to identify areas for improvement in patient care. They often lead or participate in multidisciplinary teams focused on quality improvement projects, such as reducing hospital-acquired infections or streamlining discharge processes. Regular meetings, data sharing, and education sessions are common ways they engage staff, ensuring everyone is aligned with best practices and regulatory requirements. This collaborative approach not only fosters a culture of continuous improvement but also empowers clinical staff to contribute their insights and expertise.

What is the difference between Clinical Quality Specialist Rn vs Clinical Quality Coordinator?

AspectClinical Quality Specialist RnClinical Quality Coordinator
CredentialsRegistered Nurse (RN) license, certifications in quality or healthcare standardsTypically RN or related healthcare credential, may have quality certifications
Work EnvironmentHospitals, clinics, healthcare organizations focusing on patient care qualityHealthcare settings, administrative offices, quality improvement teams
Employer & Industry UsageUsed in hospitals, healthcare systems, and clinics emphasizing clinical qualityFound in healthcare organizations focusing on quality assurance and compliance

The Clinical Quality Specialist Rn primarily focuses on clinical quality improvement, patient safety, and compliance using their nursing expertise. The Clinical Quality Coordinator often handles administrative tasks, data collection, and process improvements. Both roles support healthcare quality but differ in clinical versus administrative focus.

What are popular job titles related to Clinical Quality Specialist Rn jobs in Raleigh, NC?

For Clinical Quality Specialist Rn jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Clinical Quality Specialist Rn jobs in Raleigh, NC look for?

The top searched job categories for Clinical Quality Specialist Rn jobs in Raleigh, NC are:

Clinical Quality Specialist Rn jobs near you
Infographic showing various Clinical Quality Specialist Rn job openings in Raleigh, NC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $86,238 per year, or $41.5 per hour.

Quality Specialist III

Precision Biosciences

Durham, NC • On-site

Full-time

Re-posted 5 days ago

Job description

Summary
The Quality Specialist III is responsible for providing dedicated quality assurance support for Chemistry, Manufacturing, and Controls (CMC) operations at Precision BioSciences, including batch release review, deviation assessment, and CDMO oversight. The Quality Specialist III will work closely with QA leadership, operating with supervised independence to execute QA review activities, escalating higher-risk decisions appropriately while building proficiency in risk-based quality decision-making. This position is critical to maintaining regulatory compliance, inspection readiness, and operational continuity as the company's clinical pipeline continues to grow.
Essential Duties and Responsibilities
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position. This list contains the major duties and requirements of the job and is not all-inclusive. Incumbent(s) may be expected to perform role-related duties other than those contained in this document.
  • Support batch release review and disposition activities for CMC drug substance and drug product, including review of analytical data packages, certificates of analysis, and batch records in accordance with applicable SOPs
  • Perform deviation and investigation impact assessments for CMC-related events, documenting findings and supporting root cause analysis in the quality management system under the direction of QA leadership
  • Conduct QA review of method validation and technology transfer documentation, assay data packages, and specification verification records for CMC programs in support of PBGENE-HBV and PBGENE-DMD-01
  • Participate in CDMO technical and quality meetings, supporting oversight of contract manufacturing and testing organizations in alignment with PBI's quality requirements and supplier qualification program
  • Support the implementation and maintenance of CMC QA review checklists and standardized review frameworks to promote consistency, data integrity, and inspection readiness
  • Assist with raw data reconciliation and perform QA review of CMC release documentation packages, escalating complex or higher-risk determinations to QA leadership per defined escalation pathways
  • Maintain quality records and documentation in ZenQMS and other quality management systems, ensuring completeness, accuracy, and compliance with 21 CFR Parts 210, 211, Part 11, and applicable ICH guidelines
  • Support QA SOP training, competency development milestones, and continuous process improvement initiatives within the QA department, contributing to an environment of quality culture and regulatory compliance

Qualifications
The requirements listed below are representative of the knowledge, skill, and/or ability required to perform this job successfully.
Required:
  • B achelor's degree in Biology, Biochemistry, Chemistry, Microbiology, or a related life sciences discipline and 5+ years of relevant experience in a GMP-regulated environment, including background in quality assurance, research, or biopharmaceutical/gene therapy manufacturing, or equivalent combination of education and experience
  • Strong attention to detail in reviewing technical documentation, analytical data, and GMP records
  • Demonstrated ability to review and evaluate scientific/technical documentation with attention to detail and a commitment to data integrity
  • Familiarity with applicable regulatory requirements including 21 CFR Parts 210, 211, Part 11, and ICH Q10; ability to interpret and apply GMP requirements to day-to-day quality activities
  • Strong written and verbal communication skills; ability to clearly document quality findings and prepare concise review memos and summary reports
  • Ability to work effectively in a cross-functional team environment, prioritize competing tasks, and operate with increasing independence under QA leadership guidance

Preferred:
  • Experience in quality assurance, research, or manufacturing
  • Prior experience in a Quality Assurance role within gene therapy, cell therapy, or biologics organization
  • Experience with electronic quality management systems (e.g., ZenQMS or equivalent) for deviation, change control, and CAPA management
  • Familiarity with ICH Q10, ICH Q2(R2), or related guidance documents applicable to analytical method validation and CMC quality
  • Experience with CDMO or CRO oversight in a GMP context, including attendance at technical or quality review meetings
  • Background in analytical chemistry, molecular biology, or cell biology with hands-on laboratory experience applicable to CMC assay evaluation and validation
  • Basic understanding of GMP manufacturing processes and ability to work with subject matter experts in the context of Quality oversight of manufacturing
  • Experience participating in Quality related documentation/investigations (OOS, deviations, change controls, CAPS, etc.)

Travel Requirements
  • Minimal travel is anticipated for this position. Occasional domestic travel (estimated <10%) may be required to support CDMO site visits, supplier qualification audits, or internal training activities.

Location
  • This is an office-based position located in Durham, NC.

Precision BioSciences, Inc. (Nasdaq: DTIL), is a clinical stage biotechnology company dedicated to improving life (DTIL) with its novel and proprietary ARCUS� genome editing platform. This isn't just a statement supporting the products that we're developing � it's a statement that speaks to our collective desire to do our part in improving the lives of those around us. ARCUS is a highly specific and versatile genome editing platform designed with therapeutic safety, delivery, and control in mind. Using ARCUS, Precision is developing in vivo gene correction therapies for genetic diseases. Our team includes pioneers in genome editing, leaders in business, and a full staff of talented and committed people who are excited to be a part of medical and scientific breakthroughs. For additional information, please visit www. precisionbiosciences.com
Precision BioSciences actively fosters an inclusive environment to ensure we attract and retain the best talent; we value diversity of life experiences and perspectives; and we encourage innovation in pursuit of our mission. We provide equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state and local laws. Precision BioSciences complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

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