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Senior Statistical Programmer Jobs in Raleigh, NC

Ra

Marketing Analytics Manager

Raleigh, NC · On-site

Mid - Senior Level This is what you will do.. You will be using quantitative methods to assess the ... Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing ...

Endo International

Sr Ops Quality Eng

Raleigh, NC · On-site

$86K - $116K/yr

The Sr. Quality Engineer will provide statistical and process support to assist with continuous improvement activities. ESSENTIAL FUNCTIONS : The role provides input into regulatory filings as well ...

Endo International

Sr Ops Quality Eng

Raleigh, NC · On-site

$86K - $116K/yr

The Sr. Quality Engineer will provide statistical and process support to assist with continuous improvement activities. ESSENTIAL FUNCTIONS : The role provides input into regulatory filings as well ...

Pwc

Data Engineer - Senior Associate

Raleigh, NC

$77K - $202K/yr

As a Senior Associate, you will build meaningful client connections and learn how to manage and ... Statistics - Demonstrating proficiency in data engineering platforms like Databricks - Utilizing ...

NC SECU

Model Risk Analyst

Raleigh, NC · Hybrid

... senior validation staff. * (30%) Validate the performance and controls of statistical models using provided model development documentation and communications with model developers. Document and ...

Pharpoint Research

Director, Biostatistics

Durham, NC · On-site

Provide administrative and functional oversight for the biostatistics and statistical programming ... Provide accurate and timely status updates to other team members, colleagues, and senior management.

GSK

ViiV Healthcare (GSK) Statistics Leader

Durham, NC · On-site

... statistical programming, clinical data management, medical writing & clinical submission, for one ... Clearly communicates complex technical concepts to diverse audiences, including senior managers and ...

RTI International

Senior Biostatistician

Raleigh, NC · On-site +1

We are currently seeking a Senior Biostatistician to join our growing Biostatistics team. In this ... Ensure the quality, accuracy, and timeliness of statistical analyses and programming outputs.

RTI International

Senior Biostatistician

Raleigh, NC · On-site +1

We are currently seeking a Senior Biostatistician to join our growing Biostatistics team. In this ... Ensure the quality, accuracy, and timeliness of statistical analyses and programming outputs.

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Senior Statistical Programmer information

See Raleigh, NC salary details

$80.2K

$124.7K

$162.8K

How much do senior statistical programmer jobs pay per year?

As of Jun 21, 2026, the average yearly pay for senior statistical programmer in Raleigh, NC is $124,705.00, according to ZipRecruiter salary data. Most workers in this role earn between $104,000.00 and $143,900.00 per year, depending on experience, location, and employer.

What is a Senior Statistical Programmer job?

A Senior Statistical Programmer is responsible for developing, testing, and validating statistical programs used for clinical trial data analysis. They work primarily with statistical software like SAS to generate tables, listings, and figures (TLFs) for regulatory submissions and research studies. This role requires strong programming skills, knowledge of statistical methodologies, and an understanding of clinical trial processes. Senior Statistical Programmers also collaborate with statisticians, data managers, and regulatory teams to ensure data integrity and compliance with industry standards.

What are the key skills and qualifications needed to thrive in the Senior Statistical Programmer position, and why are they important?

To thrive as a Senior Statistical Programmer, a strong background in statistical analysis, programming (often in SAS and R), and a relevant degree such as in statistics, mathematics, or computer science is essential. Experience with regulatory submission standards (like CDISC SDTM/ADaM), clinical trial software, and certifications such as SAS Certified Advanced Programmer are highly valued. Outstanding attention to detail, problem-solving abilities, and effective communication skills help individuals excel in this collaborative and deadline-driven role. These skills are crucial for ensuring accurate data analysis, regulatory compliance, and successful teamwork in high-stakes research environments.

What are the typical responsibilities and team dynamics for a Senior Statistical Programmer?

As a Senior Statistical Programmer, you will typically be responsible for designing, developing, and validating statistical programs for clinical trial data analysis and reporting. You’ll work closely with biostatisticians, data managers, and clinical project teams to ensure data quality and regulatory compliance, often contributing to the creation of submission datasets and study reports. The role usually involves both independent work and active collaboration, with seasoned programmers frequently mentoring junior staff and participating in process improvement initiatives. This team-oriented structure offers exposure to a variety of projects and stakeholders, making it a dynamic environment ideal for those who enjoy both analytical tasks and cross-functional teamwork.

What are the most commonly searched types of Statistical Programmer jobs in Raleigh, NC? The most popular types of Statistical Programmer jobs in Raleigh, NC are:
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What cities near Raleigh, NC are hiring for Senior Statistical Programmer jobs? Cities near Raleigh, NC with the most Senior Statistical Programmer job openings:
Senior Statistical Programmer jobs near you
Sr. Lead Biostatistician - Oncology Evidence Generation

Sr. Lead Biostatistician - Oncology Evidence Generation

Labcorp

Durham, NC • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago

Labcorp rating

6.6

Company rating: 6.6 out of 10

Based on 1,100 frontline employees who took The Breakroom Quiz

78th of 103 rated laboratories

Job description

Labcorp is seeking a Senior Lead Biostatistician - Oncology Evidence Generation to join our team in Raleigh/Durham, NC.
Work Schedule: Monday - Friday, First Shift
Job Summary:
Labcorp is seeking a Senior Lead Biostatistician to join our cross-functional Evidence Generation team, supporting a growing portfolio of oncology research initiatives, with a focus on observational clinical validity studies in minimal residual disease (MRD), alongside investigator-initiated studies, registries, and real-world evidence programs. This role will serve as the statistical lead across multiple studies, driving study design, analytical strategy, and execution to ensure high-quality, scientifically rigorous outputs.
The Senior Lead Biostatistician will act as a central statistical leader, partnering closely with clinical development, scientific, data, and operational teams, as well as external investigators and collaborators. This individual will ensure studies are appropriately designed, powered, and analyzed while delivering high-quality statistical outputs that support evidence generation, publication, and clinical adoption. The role plays a critical part in translating complex data into meaningful insights and advancing Labcorp's precision oncology evidence strategy.
Job Responsibilities:
  • Contribute to and shape the design of MRD-focused studies, including clinical validity studies, registries, and real-world evidence programs, defining endpoints, analysis strategies, and overall statistical approach across multiple concurrent programs
  • Perform sample size and power calculations, support endpoint justification, and draft statistical sections of study protocols
  • Independently perform statistical analyses across diverse datasets (clinical, assay/validation, and real-world/registry data) using appropriate methods (e.g., regression, survival analysis, validation approaches), ensuring accuracy, reproducibility, and appropriate documentation
  • Serve as the statistical point of contact for assigned studies; partner with clinical, translational, and data teams, as well as external collaborators, to support study execution and communicate statistical concepts, methods, and results clearly to non-statistical stakeholders
  • Identify study risks and provide data-driven recommendations to support study integrity and decision-making
  • Develop, manage, and maintain statistical deliverables (analysis summaries, tables/listings/figures, study reports) and lead or contribute to the development of Statistical Analysis Plans (SAPs)
  • Contribute to abstracts, manuscripts, and scientific presentations supporting evidence generation and publication strategy
  • Manage statistical deliverables across multiple concurrent studies, ensuring timelines, quality, and consistency of outputs
  • Lead or contribute to development of statistical templates, tools, and workflows, while building subject matter expertise in MRD and oncology study methodologies

Minimum Requirements:
  • MS in Biostatistics, Statistics, or a related quantitative field
  • 6 or more years of experience in clinical biostatistics within biotechnology, diagnostics, CRO, or related healthcare environments
  • 5 or more years of experience in statistical programming (R, SAS or equivalent acceptable)
  • 3 or more years of experience supporting clinical research studies, including observational studies, registries, and/or assay validation efforts
  • 3 or more years of experience independently managing statistical analyses and deliverables across multiple concurrent studies

Preferred Requirements:
  • PhD in Biostatistics, Statistics, or a related quantitative field
  • 3 or more years of experience in oncology research, biomarker-driven studies, or precision oncology
  • 3 or more years of experience with real-world data, registry-based research, or observational study designs
  • 3 or more years of experience contributing to scientific publications, including abstracts, manuscripts, or conference presentations
  • 1 or more years of experience with MRD, ctDNA, genomics/NGS-based assays, or molecular diagnostics
  • 1 or more years of experience with clinical study documentation and regulatory standards (e.g., protocols, SAPs, GCP principles)

Additional Job Standards:
  • Strong foundation in clinical study design and applied statistical leadership, including sample size estimation, power calculations, and endpoint evaluation
  • Experience applying statistical methods to clinical, real-world, and/or assay validation datasets, including regression and survival/time-to-event analysis
  • Strong written and verbal communication skills, with ability to clearly convey complex statistical concepts to diverse scientific and non-technical audiences
  • Demonstrated ability to work effectively in cross-functional teams and collaborate with internal stakeholders and external partners
  • Strong analytical, problem-solving, and organizational skills, with high attention to detail and commitment to data quality and scientific rigor
  • Experience working in collaborative research environments involving academic or external investigator partnerships
  • Occasional travel for internal meetings or external collaborator engagement, as needed (≤10-15%)

Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan. For more detailed information, please click here.
Labcorp is proud to be an Equal Opportunity Employer:
Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.
We encourage all to apply
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