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Director Statistical Programming Jobs in Florida

UAB

BIOSTATISTICIAN LEAD

Tampa, FL

$73K - $120K/yr

... directing the biostatistical team, mentoring junior staff, leading grant and publication efforts ... Proficiency in statistical programming and data analysis software Experience with complex ...

TECO

Sr. Director of Pricing

Tampa, FL · On-site

Title: Sr. Director of Pricing Company: Tampa Electric Company State and City: Florida - Tampa ... Bachelor's degree in Accounting, Legal, Finance, Economics, Mathematics, Statistics, Engineering ...

TECO

Sr. Director of Pricing

Tampa, FL · On-site

Title: Sr. Director of Pricing Company: Tampa Electric Company State and City: Florida - Tampa ... Bachelor's degree in Accounting, Legal, Finance, Economics, Mathematics, Statistics, Engineering ...

U.S. Department of Defense (DOD)

$63K/yr

This is a Direct Hire Solicitation. This public notice is to gather applications that may or may ... Experience in administrative aspects of task engineering and management, e.g., procurement policies ...

U.S. Department of Defense (DOD)

$63K/yr

This is a Direct Hire Solicitation. This public notice is to gather applications that may or may ... Experience in administrative aspects of task engineering and management, e.g., procurement policies ...

US Department of the Air Force

$63K/yr

This is a Direct Hire Solicitation. This public notice is to gather applications that may or may ... Experience in administrative aspects of task engineering and management, e.g., procurement policies ...

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All JobsDirector Statistical Programming JobsDirector Statistical Programming Jobs in Florida

Director Statistical Programming information

See Florida salary details

$114.7K

$209.4K

$257.1K

How much do director statistical programming jobs pay per year?

As of Jul 5, 2026, the average yearly pay for director statistical programming in Florida is $209,352.00, according to ZipRecruiter salary data. Most workers in this role earn between $194,700.00 and $241,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Director of Statistical Programming, and why are they important?

To thrive as a Director of Statistical Programming, you need advanced expertise in statistical analysis, programming languages such as SAS or R, and a strong background in clinical trial data, typically supported by a degree in statistics, mathematics, or a related field. Familiarity with regulatory submission processes, CDISC standards, and project management tools is essential, as are relevant certifications like SAS Certified Professional. Leadership, effective communication, and strategic thinking are key soft skills for managing teams and collaborating across departments. These skills ensure high-quality data outputs, regulatory compliance, and successful execution of complex clinical development projects.

What Is the Job of a Director Statistical Programming?

The job of a director of statistical programming oversees the development and implementation of SAS programs to produce statistical analysis datasets. In this career, your responsibilities include managing the team that generates tables and graphs using the SAS programs for applications such as clinical studies. Other duties include participating in the planning and review of statistical analysis and studying reports, abstracts, and manuscripts as required. You collaborate with project leads to contribute to department operations and standards, such as CDISC for clinical research.

How does a Director of Statistical Programming typically collaborate with cross-functional teams in a pharmaceutical or biotech company?

A Director of Statistical Programming regularly works with biostatistics, clinical data management, regulatory affairs, and medical writing teams to ensure that statistical deliverables meet project timelines and regulatory requirements. They coordinate programming efforts across multiple studies, provide leadership and mentorship to programming staff, and help resolve technical or resource-related challenges. Effective collaboration is essential to streamline workflows, maintain data integrity, and ensure clear communication of statistical results within the organization.

What does a Director of Statistical Programming do?

A Director of Statistical Programming oversees teams responsible for the programming and analysis of clinical trial data, ensuring the accuracy and integrity of statistical outputs. They set departmental strategies, manage resources, and ensure compliance with regulatory requirements and industry standards. This role also involves collaborating with other departments, such as biostatistics and clinical operations, to support the successful delivery of statistical analyses for drug development and regulatory submissions. They play a key leadership role in mentoring staff and advancing programming processes and technologies.
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Director Statistical Programming jobs near you

Clinical SAS Programmer

Katalyst Healthcares and Life Sciences

Jacksonville, FL • On-site

Other

Posted 13 days ago

Job description

Responsibilities:
  • Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s)
  • Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets
  • Creates and validates tables, figures and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements
  • Provides input in the design and development of case report forms and clinical databases
  • Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs
  • Programs quality checks for clinical study raw data and report the findings to Data Management
  • Provides input in the design and development of case report forms and clinical study databases
  • Reviews or author eCRF, SDTM and ADaM datasets specifications for datasets programming
  • Provides programming support for adhoc analysis
  • Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group (e.g., macros or graphical user interface applications)
  • Manages timelines and schedules of specific phases of projects with internal personnel and external vendors
  • cts as lead programmer for a study
  • Reviews or validates statistical deliverables of vendors for assigned project(s)
Requirements:
  • MS in Statistics, Computer Science, or a related field with at least 3 years or BS in Statistics, Computer Science, or a related field with at least 5 years.
  • Experience in providing statistical programming support to early and late phase clinical trials.
  • Excellent skills in SAS programming and statistical reporting.
  • Knowledge of CDISC standards for SDTM and ADaM and FDA electronic data submission requirements.
  • Familiarity with FDA and ICH regulations and guidelines.
  • Excellent problem-solving skills.
  • Good written and verbal communication skills and organizational and documentation skills.
  • bility to work on a multidisciplinary team that may include Biostatistics, Medical Directors, Data Management, Medical Writing, Pharmacovigilance, Clinical Operations, Medical Affairs, etc.
  • bility to prioritize and multi-task effectively
  • Demonstrated positive attitude and the ability to work well with others.

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