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Associate Director Statistical Programming Jobs in Harrison, NJ

Gilead

Assoc Director, Biostatistics

Parsippany, NJ

$195K - $253K/yr

As an Associate Director, Biostatistics , at Gilead you will ... Key Responsibilities ... Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research Associates ...

Gilead

Assoc Director, Biostatistics

Parsippany, NJ · On-site

$195K - $253K/yr

As an Associate Director, Biostatistics , at Gilead you will ... Key Responsibilities ... Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research Associates ...

Altimmune

Director, Biostatistics

Morristown, NJ · On-site

Responsible for the overall quality of statistical design, programming, analysis, and data ... A self-directed individual who can excel both independently and as a team player in a fast-paced ...

Altimmune

Director, Biostatistics

Morristown, NJ · On-site

Responsible for the overall quality of statistical design, programming, analysis, and data ... A self-directed individual who can excel both independently and as a team player in a fast-paced ...

Altimmune

Director, Biostatistics

Morristown, NJ · On-site +1

Responsible for the overall quality of statistical design, programming, analysis, and data ... A self-directed individual who can excel both independently and as a team player in a fast-paced ...

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All JobsAssociate Statistical Programming JobsAssociate Director Statistical Programming JobsAssociate Director Statistical Programming Jobs in Harrison, NJ

Associate Director Statistical Programming information

See Harrison, NJ salary details

$160.8K

$293.4K

$360.3K

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

As of Jul 16, 2026, the average yearly pay for associate director statistical programming in Harrison, NJ is $293,421.00, according to ZipRecruiter salary data. Most workers in this role earn between $272,800.00 and $337,800.00 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.

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.

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 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 Harrison, NJ? For Associate Director Statistical Programming jobs in Harrison, NJ, the most frequently searched job titles are:
What job categories do people searching Associate Director Statistical Programming jobs in Harrison, NJ look for? The top searched job categories for Associate Director Statistical Programming jobs in Harrison, NJ are:
What cities near Harrison, NJ are hiring for Associate Director Statistical Programming jobs? Cities near Harrison, NJ 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 Harrison, NJ as of July 2026, with employment types broken down into 1% As Needed, 69% Full Time, 28% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $293,421 per year, or $141.1 per hour.
Associate Director, Data Operations

Associate Director, Data Operations

Artech Information System LLC

Woodcliff Lake, NJ • On-site

Full-time

Re-posted 13 days ago

Job description

Company Description

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.

Job Description

Candidate must have experience in submissions, statistical programming, EDC, SAS and CRF forms.
The Client Neuroscience Group Business is currently looking to fill an Associate Director, of Data Operations opening at its North American Headquarters in Woodcliff Lake, NJ.
The individual should have expertise in addressing technical challenges that connect EDC, SAS, CDISC and XML.
Excellent technical skills in EDC and SAS systems and application development.
Experience in consulting on projects dealing with the assessment, design and/or implementation of CDISC data standards in the clinical data life cycle at global level for both CRF standards and SDTM standards.
Experience in Review and Quality assurance of datasets and programming specifications produced by other programmers.
Experience in Accountability for development and maintenance of cross-functional / cross-department process related to clinical trials SDTM data production, including specification, programming, QC, and deliverables of SDTM data for analyses and submissions. Responsible for implementing new technologies for end users and streaming the process from data collection to submission.
Scope and Responsibilities:
- A highly specialized individual contributor or functional manager with advanced knowledge and expertise in a professional discipline.
- Leads execution of key business objectives or projects within the department.
- Involved in developing, modifying, and executing company policies that affect immediate operations and may also have company-wide effect.
The individual must have the following skills:
Expertise in addressing technical challenges that connect EDC, SAS, CDISC and XML.
Excellent technical skills in SAS system and application development.
Proven experience in development and implementation of clinical standards in a global pharmaceutical environment.
Expert in integrating SAS with other leading technologies such as PDF, XML, Microsoft Office, to support electronic submissions.
Experience in consulting on projects dealing with the assessment, design and/or implementation of CDISC data standards in the clinical data life cycle.
Experience in Annotating CRFs in accordance with CDISC published or company specific guidelines with appropriate metadata to reflect case report tabulation data sets.
Experience in Reviewing and quality assurance of CRF annotations produced by other programmers
Embracing and contributing to our culture of process improvements with a focus on streamlining our processes adding value to our business needs.
Experience in Reviewing and quality assurance of datasets, programs and programming specifications produced by other programmers.
Accountability for development and maintenance of cross-functional / cross-department process related to clinical trials SDTM data production, including specification, programming, QC, and deliverables of SDTM data for analysis and submission.
Accountability for execution of process related to clinical trials SDTM data production, including specification, programming, QC, and deliverables of SDTM data for analysis and submission
Engaging appropriate stakeholders in communication to create SDTM standards and process for transition of clinical data to SDTM
Accountability for SDTM datasets specification, conversion, and delivery to stakeholders, specifically Statistical Programming, but also other users of SDTM datasets, with high quality and on time.
Providing SDTM data production technology to CDO (Clinical Data Operations) related to SDTM data delivery and manages the activities of a team with a common focus.

Additional Information

For more information, Please contact

Mayank Sharma

973-967-3431

mayank(DOT)sharma1@artecinfo(DOT)com

Artech logo

About Artech

Sourced by ZipRecruiter

Artech is a leading IT staffing and consulting company based in Morristown, NJ, US. Since its foundation in 1992, Artech has mastered in complementing human expertise with technology and business acumen to produce world-class staffing solutions. The company caters to diverse industry sectors, including financial services, healthcare, telecommunication, energy and utilities, supply chain, and retail. It provides IT consulting, project management, professional and staff augmentation, and managed staffing services. Artech's mission is to provide exceptional IT staffing services to its clients by comprehending their business needs and then crafting a customized staffing strategy. Its notable achievement includes being recognized as one of the largest IT staffing companies in the U.S, according to Staffing Industry Analysts (SIA).

Industry

Recruiting and staffing services

Company size

10,000+ Employees

Headquarters location

Morristown, NJ, US

Year founded

1992

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