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Associate Director Statistical Programming information

See Florida salary details

$114.7K

$209.4K

$257.1K

How much do associate director statistical programming jobs pay per year?

As of Jun 27, 2026, the average yearly pay for associate 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 an Associate Director Statistical Programming, and why are they important?

To thrive as an Associate Director Statistical Programming, you need expertise in statistical programming, clinical trial data standards, and a degree in statistics, mathematics, or a related field, often with several years of experience in the pharmaceutical or biotechnology industry. Proficiency in programming languages such as SAS and R, knowledge of CDISC standards (SDTM, ADaM), and familiarity with regulatory submission requirements are typically required. Strong leadership, project management, and communication skills are vital for guiding teams and collaborating with cross-functional partners. These skills and qualities ensure the delivery of high-quality, compliant statistical outputs that support clinical development and regulatory approval.

How to become a director of statistical programming?

To become a director of statistical programming, professionals typically need extensive experience in statistical programming, often 8-10 years, with a strong background in biostatistics, data analysis, and programming languages like SAS or R. Advancing usually requires demonstrating leadership skills, managing teams, and understanding regulatory requirements; obtaining relevant certifications and a master's or doctoral degree can also support career progression.

What does an Associate Director of Statistical Programming do?

An Associate Director of Statistical Programming leads teams responsible for the design, development, and validation of statistical programs used in the analysis of clinical trial data. They oversee the creation of datasets, tables, listings, and figures that support regulatory submissions and scientific publications. In addition to technical expertise, this role involves managing timelines, ensuring compliance with regulatory standards, and collaborating with cross-functional teams such as biostatistics, data management, and clinical operations.

Is an associate director a high level position?

An Associate Director in statistical programming is considered a senior-level position within an organization, often responsible for overseeing project teams, managing timelines, and ensuring regulatory compliance. It typically requires several years of experience and advanced skills in programming languages like SAS or R, along with leadership abilities. This role is generally regarded as a high-level management position in the industry.

How much does a statistical programmer earn?

A statistical programmer's salary varies based on experience, location, and industry, but typically ranges from $70,000 to $120,000 annually. Senior roles or those with specialized skills in programming languages like SAS or R can earn higher salaries, especially in the pharmaceutical or biotech sectors.

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

As an Associate Director of Statistical Programming, you will work closely with biostatisticians, clinical data managers, and regulatory affairs professionals to ensure that statistical analyses and data outputs meet project and regulatory requirements. You’ll often lead programming teams, coordinate timelines, and help translate statistical analysis plans into executable code. Regular meetings and clear communication are key, as you’ll be expected to provide technical guidance and ensure data integrity across multiple studies or programs. This role often requires balancing hands-on programming with strategic leadership and mentorship responsibilities.

How much does a Pfizer statistical programming manager make?

A Pfizer statistical programming manager typically earns between $120,000 and $160,000 annually, depending on experience, location, and level within the company. Compensation may also include bonuses and benefits, and strong skills in SAS, R, or Python are often required for the role.

What is the difference between Associate Director Statistical Programming vs Statistical Programmer?

AspectAssociate Director Statistical ProgrammingStatistical Programmer
Required CredentialsBachelor's or Master's in Biostatistics, Statistics, or related field; experience in clinical trial programmingBachelor's or Master's in similar fields; entry to mid-level experience
Work EnvironmentLeads teams, manages projects, collaborates with cross-functional teamsPerforms programming tasks, supports project teams, executes statistical analyses
Employer & Industry UsagePharmaceutical and biotech companies, clinical research organizationsPharmaceutical companies, CROs, biotech firms

The Associate Director Statistical Programming typically oversees programming teams and manages project deliverables, requiring leadership skills and extensive experience. In contrast, the Statistical Programmer focuses on executing programming tasks under supervision. Both roles are essential in clinical research, but the Associate Director holds more managerial responsibilities and strategic oversight.

What are popular job titles related to Associate Director Statistical Programming jobs in Florida? For Associate Director Statistical Programming jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Associate Director Statistical Programming jobs in Florida look for? The top searched job categories for Associate Director Statistical Programming jobs in Florida are:
What cities in Florida are hiring for Associate Director Statistical Programming jobs? Cities in Florida with the most Associate Director Statistical Programming job openings:
Associate Director Statistical Programming jobs near you

Biostatistical Prograrmming Manager

Amgen

Jacksonville, FL • On-site

Full-time

Posted 12 days ago

Job description

Career CategoryClinicalJob Description

Biostatistical Programming Manager

What you will do

Let's do this. Let's change the world. In this vital role you will provide both strategic oversight and hands-on statistical programming support to enable high-quality and timely clinical trial deliverables.

This role is part of the centrally managed Quality and Quick Response (QQR) Programming team and is responsible for supporting urgent and high-priority programming needs across development programs. The manager will serve as a technical programming expert who can rapidly respond to internal and external requests, support special projects, provide global quality oversight, and contribute directly to programming deliverables when needed.

This role will primarily support programs within the Obesity Therapeutic Area and requires close collaboration with cross-functional teams to support fast-paced development activities and evolving business priorities.

Responsibilities

Provide rapid response statistical programming support for urgent internal and external requests

Serve as a lead programmer for studies and projects, such as Data Access Plan (DAP) activities, unblinding efforts, and special projects

Deliver hands-on programming support for SDTM, ADaM, Tables, Listings, and Figures (TFLs), and other study and regulatory submission deliverables as needed

Oversee the execution and quality of projects managed by our FSP partners per Amgen Global Statistical Programming (GSP) Quality Oversight Plan (QOP)

Ensure that FSP and in-house programming deliverables meet quality, compliance, timeline, and productivity expectations

Mitigate at-risk projects by providing technical expertise, programming support, and operational guidance

Contribute to training material development and delivery to internal teams and FSP partners

Provide guidance and technical consultancy to study programming team on Amgen processes, tools, and utilities

Lead/contribute to GSP continuous improvement iniatives and support cross-functional initiatives including inspection readiness, process improvement, innovation, and training activities

Contribute to programming team performance metrics development, data collection, and reporting

Review project documentation such as specifications, issue logs, deliverable status for accuracy and completeness

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a manager with these qualifications.

Basic Qualifications:

Doctorate degree OR

Master's degree and 2 years of statistical programming experience OR

Bachelor's degree and 4 years of statistical programming experience OR

Associate's degree and 8 years of statistical programming experience OR

High school diploma / GED and 10 years of statistical programming experience

Preferred Qualifications:

Masters in Computer Science, Statistics, Mathematics, Computer Science, Life Sciences or another relevant scientific subject

6+ years of statistical programming in biopharmaceutical industry

Regulatory submission experience

Strong hands-on SAS programming expertise including SAS Base, Macro, SQL, SAS/Graph and Stat packages

Experience with R programming for clinical trial analyses, data manipulation, reporting and visualization preferred

Familiarity with additional programming languages and tools such as Python preferred

Hands-on experience developing and validating SDTM, ADaM datasets, and TFLs

Thorough understanding of clinical trial processes from data collection through analysis and reporting

Ability to lead programmers in successful completion of all study programming activities and provide guidance on technical and process questions

Strong understanding of data standards and compliance checks including Pinnacle 21

Experience providing quality oversight for outsourced and internal programming deliverables

Ability to troubleshoot complex technical issues and turnaround at-risk projects

Experience working in a globally dispersed team on Phase 1-4 clinical trials

Experience supporting clinical development programs within the Obesity Therapeutic Area preferred

Understanding of obesity clinical endpoints, data standards, and regulatory considerations is highly desirable

Excellent oral and written English communication skills; strong collaboration, negotiation, and organizational skills

.

Salary Range

129,056.35USD -174,605.65USD

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