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Senior Statistical Analyst Jobs (NOW HIRING)

Navitas Life Sciences

Senior Statistician

$89K - $109K/yr

The Senior Statistician MS performs high-level client statistical consulting and/or leads teams ... Perform Statistical Analysis in support of Phase I-V clinical trials, ISS, ISE, Registries ...

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How much do senior statistical analyst jobs pay per year?

As of Jun 21, 2026, the average yearly pay for senior statistical analyst in the United States is $99,008.00, according to ZipRecruiter salary data. Most workers in this role earn between $87,000.00 and $107,000.00 per year, depending on experience, location, and employer.

What are Senior Statistical Analysts?

Senior Statistical Analysts are experienced professionals who use advanced statistical methods to collect, analyze, and interpret complex data sets. They often design experiments, develop predictive models, and provide data-driven insights to support business decision-making. In addition to technical expertise, they may oversee junior analysts, collaborate with other departments, and present findings to stakeholders. Their work helps organizations understand trends, measure performance, and identify opportunities or risks.

What are the key skills and qualifications needed to thrive as a Senior Statistical Analyst, and why are they important?

To thrive as a Senior Statistical Analyst, you need advanced knowledge of statistical theory, data analysis, and a relevant degree in statistics, mathematics, or a related field. Expertise with statistical software such as SAS, R, Python, and experience with data visualization tools are commonly required, along with certifications like SAS Certified Advanced Analytics Professional. Strong problem-solving abilities, attention to detail, and effective communication skills help you translate complex data into actionable insights. These skills ensure accurate analysis, informed decision-making, and clear communication of findings to stakeholders.

How does a Senior Statistical Analyst typically collaborate with cross-functional teams on large projects?

Senior Statistical Analysts often work closely with professionals from departments such as data engineering, product management, and business analytics. They translate complex statistical findings into actionable insights, ensuring that technical results are accessible to non-technical stakeholders. Collaboration may involve regular meetings, joint project planning sessions, and iterative feedback loops to refine analyses based on shifting business priorities. This collaborative environment not only enhances project outcomes but also provides opportunities for professional growth through exposure to diverse perspectives and expertise.
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Senior Statistical Analyst jobs near you
Infographic showing various Senior Statistical Analyst job openings in the United States as of June 2026, with employment types broken down into 64% Full Time, 31% Part Time, 3% Temporary, 1% Contract, and 1% Nights. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $99,008 per year, or $47.6 per hour.
Senior Statistical Programmer Consultant (Oncology) Remote

Senior Statistical Programmer Consultant (Oncology) Remote

ClinChoice

Remote

Full-time

Posted 3 days ago

Job description

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both worlds...
ClinChoice is searching for a Senior Statistical Programmer Consultant to join one of our clients.
The Senior Statistical Programmer will serve as a senior technical expert responsible for end-to-end programming deliverables, study leadership, and oversight of internal teams and external vendors. This role requires advanced expertise in SAS, familiarity with R, deep knowledge of CDISC standards, and strong experience working on oncology studies and regulatory submissions.
Key Responsibilities
Technical Leadership
  • Lead programming activities for oncology clinical trials across multiple studies.
  • Develop, validate, and maintain SDTM and ADaM datasets following CDISC guidelines.
  • Oversee production of Tables, Listings, and Figures (TLFs) for study reporting and submissions.
  • Provide SAS programming expertise to support complex data derivations and analyses.
  • Review and ensure traceability, consistency, and quality of all programming deliverables.
Project & Study Management
  • Act as programming lead for assigned studies, managing timelines and deliverables.
  • Work closely with Biostatistics, Data Management, Medical Writing, and Regulatory Affairs.
  • Coordinate with CROs and external vendors, ensuring compliance, quality, and adherence to client programming standards.
  • Support integrated analyses including ISS/ISE.
Regulatory & Submission Support
  • Prepare submission-ready programming outputs and documentation, including define.xml, annotated CRFs, and reviewer guides.
  • Ensure all programming meets regulatory requirements (FDA, EMA, PMDA).
  • Contribute to responses for regulatory queries and data requests.

Required Qualifications
  • Bachelor's or Master's degree in Statistics, Computer Science, Mathematics, Life Sciences, or related field.
  • 8-12+ years of statistical programming experience in pharma/biotech or CRO.
  • Expert-level proficiency in SAS.
  • Strong understanding of CDISC SDTM and ADaM standards.
  • Significant experience supporting oncology clinical trials (hematologic or solid tumors).
  • Experience supporting regulatory submissions and preparing submission-ready outputs.
  • Excellent communication skills and ability to collaborate cross-functionally.

The Application Process
Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
Who will you be working for?
About ClinChoice
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Our Company Ethos
Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.
ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.

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