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Associate Director Statistical Programming Jobs in Florida

CMC Statistics Assoc Dir What you will do Let's do this. Let's change the world. In this vital role ... Proficient in SAS programming (data manipulation techniques, macro, statistical and graphical PROCs ...

UCF's College of Engineering and Computer Science is one of the largest and most dynamic ... Stat. 112.219(6). Preferred Qualifications : * Demonstrated success identifying, cultivating, and ...

Associate Director

Jacksonville, FL · On-site

$120 - $160/hr

... engineering, automation, data engineering, and infrastructure modernization services, while ... Position Description Bridgenext, Jacksonville, FL, seeks Associate Director to lead, guide ...

## Associate Director, #Brand DesignApplylocations: Orlando, FL (Main Campus)time type: Full ... programming* Paid time off for applicable positions, including annual and sick time off and paid ...

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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 Sep 2, 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 does an associate director 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.

What are the key skills and qualifications needed to thrive as an associate director statistical programming?

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 does an associate director 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.

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:

Infographic showing various Associate Director Statistical Programming job openings in Florida as of August 2026, with employment types broken down into 100% Full Time. Highlights an 60% In-person, and 40% Hybrid job distribution, with an average salary of $209,352 per year, or $100.7 per hour.

CMC Statistics Assoc Dir

Amgen

Miami, FL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 5 days ago


Job description

Career CategoryOperationsJob DescriptionJoin Amgen's Mission of Serving Patients

At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do.

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

CMC Statistics Assoc Dir

What you will do

Let's do this. Let's change the world. In this vital role you will contribute to Amgen's pipeline of new molecules and commercial products, that are treating serious illnesses and transforming lives.

The Associate Director will be a member of the Global CMC Statistics (GCS) team. The mission of the team is to design, develop and promote best practices, processes and tools across Operations that drive consistency and enhance compliance. As part of the Global CMC Statistics team, the Associate Director will use their expertise to implement statistical tools and techniques to support product manufacturing and testing throughout the product life cycle. The statistician will also provide support to clinical and commercial manufacturing sites in the network. This involves statistical support for monitoring programs, analytical methods, and investigations. Ad-hoc statistical support will be provided for root-cause analysis for protocol or method deviations.

The Associate Director will support the development of delivery devices, and provide statistical analysis, study designs, acceptance sampling plans and acceptance criteria for the development, qualification, and transfer of physical test methods. They will also establish appropriate study designs and carry out evaluation of acceptance criteria for Design Verification testing ensuring that the overall program is compliant with Amgen and Regulatory/ISO requirements, and support component and material qualifications using process capability analysis and equivalence tests.

Finally, the candidate will contribute to continuous improvement efforts across Amgen's networks, leading to harmonization, efficiency gains and scientific innovation and administration of statistical training for Amgen's engineers and scientists.

  • Drive improvements/standardization in one or more key areas of statistical analysis
  • Use Amgen-provided Artificial Intelligence (AI) tools to enhance existing business processes
  • Reviews and provides quality oversight of technical documents.
  • Supports the development and review of SOPs and other controlled documents within Amgen or CROs for process improvement and operational efficiency.
  • Guides the development, implementation and maintenance of statistical tools used to support product life cycle activities, such as drafting/updating white papers, writing standardized SAS code, outlining report templates, and aligning GCS duties in relevant SOPs.
  • Drives statistical thinking as a leader of cross functional teams
  • Drives the development and implementation of innovative strategies and technologies in a cross functional role.
  • Considered a business or scientific-technical SME.
  • Responsible for staying up to date on scientific and industry trends, developing new techniques and plans, and understanding company goals and competitor practices.
  • Have advanced disciplinary and basic industry knowledge, in-depth understanding of project management techniques and business interdependencies, and the ability to contribute to scientific and innovative advances in the field.
  • Participate in external conferences, as appropriate, and be aware of the guidance documents and best practices in the biotechnology industry.
What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The highly motivated professional we seek is a passionate individual with these qualifications.

Basic Qualifications:

  • Doctorate degree and 3 years of Applied Statistics, Industrial Statistics or Non-clinical Biostatistics experience
    OR
  • Master's degree and 5 years Applied Statistics, Industrial Statistics or Non-clinical Biostatistics experience
    OR
  • Bachelor's degree and 7 years of Applied Statistics, Industrial Statistics or Non-clinical Biostatistics experience
    OR
  • Associate's degree and 12 years of Applied Statistics, Industrial Statistics or Non-clinical Biostatistics experience
    OR
  • High school diploma / GED and 14 years of Applied Statistics, Industrial Statistics or Non-clinical Biostatistics experience

Preferred Qualifications:

  • Advanced degree in Applied or Industrial Statistics with 5 years' experience applying statistical methodologies to Biopharma manufacturing and control
  • Proficient in statistical tools and techniques commonly used in biopharma manufacturing operations, such as, Design of Experiments, Statistical Process Control, Process Capability Analysis, Measurement System Analysis, Acceptance Sampling Plans, Non-linear and Linear Regression, Significance Tests, and Simulation.
  • Proficient in SAS programming (data manipulation techniques, macro, statistical and graphical PROCs, and ODS) and JMP statistical software
  • Excellent interpersonal, oral, and written communication skills
What you can expect of us

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way.

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

  • A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental & vision coverage, and life & disability insurance
  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
  • Stock-based long-term incentives
  • Award-winning time-off plans
  • Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.
Apply now and make a lasting impact with the Amgen team.careers.amgen.com

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

Sponsorship

Sponsorship for this role is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

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Salary Range

167,899.65USD -227,158.35USD