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Associate Director Statistical Programming Jobs in Delaware

The S&E Associate Director will set direction and lead the planning, development, and periodic ... Bachelor's degree in environmental science, occupational health and safety, engineering, or related ...

The S&E Associate Director will set direction and lead the planning, development, and periodic ... Bachelor's degree in environmental science, occupational health and safety, engineering, or related ...

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Associate Director Statistical Programming information

See Delaware salary details

$153.6K

$280.4K

$344.3K

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

As of May 30, 2026, the average yearly pay for associate director statistical programming in Delaware is $280,389.00, according to ZipRecruiter salary data. Most workers in this role earn between $260,700.00 and $322,800.00 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 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.

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.

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 Delaware? For Associate Director Statistical Programming jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Associate Director Statistical Programming jobs in Delaware look for? The top searched job categories for Associate Director Statistical Programming jobs in Delaware are:
What cities in Delaware are hiring for Associate Director Statistical Programming jobs? Cities in Delaware with the most Associate Director Statistical Programming job openings:
Infographic showing various Associate Director Statistical Programming job openings in Delaware as of May 2026, with employment types broken down into 100% Full Time. Highlights an 56% In-person, 7% Hybrid, and 37% Remote job distribution, with an average salary of $280,389 per year, or $134.8 per hour.
Statistical Science Director

Statistical Science Director

AstraZeneca

Wilmington, DE

Full-time

Posted 7 days ago


AstraZeneca rating

8.6

Company rating: 8.6 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

16th of 70 rated pharmaceutical


Job description

The Director, Statistics has sufficient experience in the pharmaceutical industry to independently lead a biometrics team to deliver project and/or technical level activities related to design, delivery and interpretation, high level internal governance committees and/or regulatory submissions. This individual is able to lead, perform and communicate results of more technical analyses, and able to guide and lead less experienced staff. Competent individual contributor with excellent cross-functional collaboration.

Accountabilities:

The Director, Statistics may lead, manage, and develop a group of statisticians as well as provide project support and/or advance statistical methodology.

The accountabilities for supporting projects directly include:

To lead, manage and develop a group of statisticians

Work according to agreed functional and regional SHE strategy by ensuring proper management of SHE risks, incidents, reporting, follow-up and improvements

Lead the statistical design and strategy to product development plans, preclinical studies, regulatory strategy, health technology assessment and/or commercial activities as appropriate for the stage of the product.

Lead the statistical content and ensure quality for study designs, documents, delivery and interpretation and submission

Quantify the benefit, risk, value and uncertainty of the emerging product profile and can communicate these effectively within the team

Provide global leadership to others and direct project work delivered by internal and external staff

Partner with CROs to ensure delivery to quality and time Represent AZ externally which may include health authorities, advisory boards, conferences, workshops and/or payer interactions

Maintain knowledge of statistical methodology in relevant areas and promote, investigate and implement novel statistical approaches

Represent statistical strategy and decision making at internal decision-making governance including review boards, therapy area leadership teams and ESPC/LSPC

Mentor/coach and support the technical education and training of Statistics staff

Essential Requirements:

  • MSc in Statistics, Mathematics (containing a substantial statistical component), or recognised equivalent to stats MSc
  • Track record of background in leading independently
  • Exemplary technical skills

Desired Requirements:

  • PhD in Statistics

Join the team unlocking the power of what science can do. We are working towards treating, preventing, modifying and even curing some of the world's most complex diseases. Here we have the potential to grow our pipeline and positively impact the lives of billions of patients around the world. We are committed to making a difference by fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs. Our combination of curiosity and courage drives us to explore new possibilities without fear of failure. We celebrate our successes and learn from our failures along the way. Our inclusive environment allows us to work seamlessly as one team, using diverse global knowledge to create the greatest impact on disease.

If your passion is science and you want to be part of a team that makes a bigger impact on patients' lives, then there's no better place to be. Apply now!

Date Posted

22-May-2026

Closing Date

26-Jun-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.


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