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Clinical Statistical Programmer Jobs in Florida (NOW HIRING)

... statistical analyses. * Strong SAS programming, SAS base, SAS macro experience. * Thorough knowledge and understanding of clinical data preferred. * Strong experience with data and production of TLGs.

FLBHC offers unique and individualized programming for adolescents and adults that sets us apart ... Ability to work with mathematical concepts such as probability and statistical inference. Ability ...

New

Assists in writing statistical analysis plans and system programming plans for all phases of clinical studies. Supports the basic activities of clinical study design related to the implementation of ...

Hospital Epic Systems BI Developer

Miami Beach, FL · On-site

  • Medical

  • Life

  • Retirement

  • PTO

In delivering an unmatched level of clinical expertise, our medical center is committed to ... economics, engineering, statistics, operations research, etc.) or equivalent experience

Process Engineer

Pinellas Park, FL · On-site

$37 - $42/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Statistical analysis experience (e.g., JMP) and ability to apply DOE, SPC, and capability studies ... We deliver agile, scalable talent solutions across IT, engineering, life sciences, clinical, and ...

Process Engineer

Pinellas Park, FL · On-site

$37 - $42/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Statistical analysis experience (e.g., JMP) and ability to apply DOE, SPC, and capability studies ... We deliver agile, scalable talent solutions across IT, engineering, life sciences, clinical, and ...

Showing results 41-60

Clinical Statistical Programmer information

See Florida salary details

$12

$40

$67

How much do clinical statistical programmer jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for clinical statistical programmer in Florida is $40.49, according to ZipRecruiter salary data. Most workers in this role earn between $25.67 and $60.91 per hour, depending on experience, location, and employer.

What are some common challenges faced by clinical statistical programmers when working with clinical trial data?

Clinical Statistical Programmers often encounter challenges such as handling large and complex datasets, ensuring data integrity, and adhering to strict regulatory guidelines (like CDISC standards). Collaborating closely with biostatisticians, data managers, and clinical teams is essential to resolve data discrepancies and meet tight project deadlines. Staying updated on evolving regulatory requirements and software tools is also vital to maintain high-quality deliverables in a fast-paced environment.

What are the key skills and qualifications needed to thrive as a clinical statistical programmer, and why are they important?

To thrive as a Clinical Statistical Programmer, you need strong proficiency in statistical programming languages (such as SAS or R), a background in statistics or life sciences, and familiarity with clinical trial processes. Experience with CDISC standards (SDTM, ADaM), regulatory submission requirements, and version control systems is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for collaborating with cross-functional teams and ensuring data quality. These skills ensure the accurate analysis and reporting of clinical data, which is critical for regulatory compliance and successful clinical trial outcomes.

What does a clinical statistical programmer do?

A Clinical Statistical Programmer is responsible for managing and analyzing clinical trial data using statistical software, such as SAS or R. Their primary tasks include creating datasets, programming statistical analyses, and generating tables, listings, and figures for clinical study reports. They work closely with biostatisticians and clinical research teams to ensure data accuracy and regulatory compliance. Their work is essential for supporting submissions to regulatory agencies and for making data-driven decisions in clinical research.

What does a clinical statistical programmer do?

The job duties of a clinical statistical programmer involve collecting data, performing statistical analysis, and analyzing data sets according to the needs of their employer or client. Your responsibilities in this career may involve using SAS programming to create and analyze data sets during clinical trials or other clinical experiments and studies. You may also be involved in performing data integration for reports following clinical research or statistical analysis for quality control (QC).

What are popular job titles related to Clinical Statistical Programmer jobs in Florida?

For Clinical Statistical Programmer jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Clinical Statistical Programmer jobs in Florida look for?

The top searched job categories for Clinical Statistical Programmer jobs in Florida are:

What are popular job titles related to Clinical Statistical Programmer jobs in FL?

For Clinical Statistical Programmer jobs in FL, the most frequently searched job titles are:

Infographic showing various Clinical Statistical Programmer job openings in Florida as of August 2026, with employment types broken down into 2% As Needed, 74% Full Time, 17% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $84,216 per year, or $40.5 per hour.

Executive Director, Clinical Data Science

Eisai

Jacksonville, FL • On-site

Full-time

Re-posted 17 days ago


Job description

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer's disease. As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile, we want to hear from you.

We are seeking a visionary leader to shape and drive Clinical Data Science strategy across our global clinical development portfolio. This role ensures the rigorous application of statistical principles and advanced data science methodologies to optimize clinical trial efficiency and accelerate innovation. The Executive Director will spearhead the integration of AI/ML solutions for applications in disease diagnosis, modeling, imaging, genomics, proteomics, and precision medicine. Acting as the primary data science representative to global regulatory authorities, this individual will defend strategies and influence industry standards.

Strategic Leadership:

  • Define and execute Clinical Data Science strategies for clinical studies and development plans across the portfolio.
  • Serve as the primary spokesperson for Data Science at Health Authority meetings, leading preparation of responses and influencing regulatory perspectives.

Innovation & Execution:

  • Drive adoption of cutting-edge AI/ML methodologies for disease modeling, biomarker analysis, and precision medicine.
  • Oversee multiple large-scale, critical data science initiatives, ensuring timely, high-quality deliverables aligned with industry best practices.

Risk Management & Problem Solving:

  • Evaluate analytical options, proactively identify risks, and develop novel solutions to complex challenges.

Thought Leadership & External Engagement:

  • Represent the organization at technical seminars and conferences; build networks with industry experts to advance best practices.

Team Leadership & Development:

  • Manage and mentor a diverse team of data scientists and people managers across geographies.
  • Foster career growth through open dialogue, performance management, and strategic development planning.

Operational Excellence:

  • Ensure GxP compliance in data science programming for clinical trials.
  • Manage budgets, vendor relationships, and third-party deliverables to maintain quality and efficiency.

Executive Communication:

  • Deliver clear, compelling communication of complex data science concepts to internal and external stakeholders with executive presence.

Qualifications

  • Ph.D. in Biostatistics or a Master's Degree in Biostatistics in combination with a Ph.D.in Bioinformatics or related computational sciences.
  • Deep expertise in statistical methods and their application in clinical trials.
  • Minimum 10 years of industry experience in clinical development, including Data Science and Biostatistics.
  • Recognized thought leader in at least one data science discipline (e.g., AI/ML modeling, precision medicine).
  • Proven experience presenting at external forums and influencing regulatory authorities.
  • Strong people leadership experience in a Data Science setting.
  • Prior research experience in neurology, particularly Alzheimer's disease biomarkers (plasma, CSF, imaging), strongly preferred.

Eisai Salary Transparency Language:

The annual base salary range for the Executive Director, Clinical Data Science is from :$273,200-$358,600Under current guidelines, this position is eligible to participate in : Eisai Inc. Annual Incentive Plan & Eisai Inc. Long Term Incentive Plan.

Final pay determinations will depend on various factors including but not limited to experience level, education, knowledge, and skills.

Employees are eligible to participate in Company employee benefit programs. For additional information on Company employee benefits programs, visit https://careers.eisai.com/us/en/compensation-and-benefits.

Certain other benefits may be available for this position, please discuss any questions with your recruiter.

Eisai is an equal opportunity employer and as such, is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran status. Similarly, considering the need for reasonable accommodations, Eisai prohibits discrimination against persons because of disability, including disabled veterans.

Eisai Inc. participates in E-Verify. E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States. Please click on the following link for more information:

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About Eisai

Sourced by ZipRecruiter

Eisai is a global pharmaceutical company (headquartered in Woodcliff Lake, NJ, US), renowned for its innovative research and development in neuroscience and oncology. The primary focus of the company is to provide therapeutic treatments and solutions for diseases like Alzheimer's, cancer, and other neurological disorders. Eisai was founded in Japan in 1941 and has since developed a strong presence across international markets. Eisai's core values center around their philosophy of 'human health care' (hhc), where they aim to make significant and positive contributions to patients and their families' healthcare worldwide.

Company size

1,001 - 5,000 Employees

Headquarters location

Nutley, NJ, US

Year founded

1995

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