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Associate Director Statistical Programming Jobs in Durham, NC

Pharpoint Research

Director, Biostatistics

Durham, NC · On-site

Provide administrative and functional oversight for the biostatistics and statistical programming (BioSP) functions of the organization. Works with Executive Director and/or Chief Scientific Officer ...

GSK

Principal Statistical Programmer

Durham, NC · On-site

As the Senior Medical Director , you will play a pivotal role in advancing our mission to leave no ... Lead programming for studies, ensuring efficient development and validation of analysis packages.

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All JobsAssociate Director Statistical Programming JobsAssociate Director Statistical Programming Jobs in Durham, NC

Associate Director Statistical Programming information

See Durham, NC salary details

$148.3K

$270.7K

$332.4K

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

As of Jun 16, 2026, the average yearly pay for associate director statistical programming in Durham, NC is $270,708.00, according to ZipRecruiter salary data. Most workers in this role earn between $251,700.00 and $311,600.00 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.

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What cities near Durham, NC are hiring for Associate Director Statistical Programming jobs? Cities near Durham, NC with the most Associate Director Statistical Programming job openings:
Associate Director Statistical Programming jobs near you
Infographic showing various Associate Director Statistical Programming job openings in Durham, NC as of June 2026, with employment types broken down into 100% Full Time. Highlights an 80% In-person, and 20% Remote job distribution, with an average salary of $270,708 per year, or $130.1 per hour.
Sr. Director, Statistical Programming Safety

Sr. Director, Statistical Programming Safety

Penfield Search Partners

Raleigh, NC • Hybrid

Other

Posted 13 days ago

Job description

Job Description Contact: Lauren Scutero - lscutero@penfieldsearch.com This is a permanent, hybrid position in Raleigh, NC with two days (Monday, Friday) as optional work from home with core collaboration days in the office: Tues, Wed, Thurs. Fully home-based work is not available for this role. Job Description Position Summary Provides strategic, operational, and hands on (player coach) leadership for compound level safety statistical programming and aggregate safety reporting deliverables, including DSUR, PSUR/PBRER, Risk Management Plan (RMP), IBRSI, and support for broader safety surveillance and safety analytics

Leads teams and oversees vendors to ensure timely, high quality, and inspection ready delivery while driving modernization through AI enabled and automated programming approaches. Key Responsibilities Lead end to end programming strategy and execution for compound level aggregate safety reporting deliverables (DSUR, PSUR/PBRER, RMP, IBRSI). Provide strategic oversight of roles, responsibilities, and build steps for aggregate safety programming delivery.

Serve as escalation point for complex pooled/cumulative safety analyses and urgent ad hoc safety requests. Maintain hands on engagement to ensure technical correctness, reproducibility, and delivery reliability for critical outputs. Ensure consistent processes, folder structures, and operational readiness for safety programming deliverables.

Own and continuously improve quality management practices, including definition and monitoring of KPIs. Provide vendor/FSP oversight and governance, ensuring training readiness, documented expectations, and appropriate QC. Lead, mentor, and develop Safety Statistical Programming staff; oversee less experienced colleagues and contribute to development of standards, tools, and templates.

Drive adoption of AI enabled and automated programming approaches to improve efficiency, consistency, and quality. Capabilities & Requirements Excellent written and verbal communication; strong influencing and negotiation skills. Deep knowledge of drug development, regulatory expectations, and industry standards for safety programming and reporting.

Proven ability to lead people leaders, delegate effectively, coach performance, and support career development. Strong judgment and problem solving skills in complex situations; ability to prioritize critical issues. Demonstrated ability to work cross functionally and influence decision making.

Education & Experience Bachelor's degree or higher in Biostatistics, Computer Science, or related field with 12+ years of relevant industry experience. 6+ years of leadership or cross functional project management experience, including managing project teams. Significant line management experience with a proven record of hiring and developing high performing talent.

Extensive experience with SAS; experience with R and/or Python preferred. Demonstrated leadership in change management and standards adoption.

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