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Director Statistical Programming Jobs in Passaic, NJ

Gilead

Director, Biostatistics

Parsippany, NJ

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

As a Director of Biostatistics at Gilead, you will... Requirements: * Provide Statistical ... Works collaboratively with Statistical Programming, Biostatistics, Clinical Research, Clinical Data ...

Gilead

Director, Biostatistics

Parsippany, NJ

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

As a Director of Biostatistics at Gilead, you will... Requirements: * Provide Statistical ... Works collaboratively with Statistical Programming, Biostatistics, Clinical Research, Clinical Data ...

Gilead

Director, Biostatistics

Parsippany, NJ

$226K - $292K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

Works collaboratively with Statistical Programming, Biostatistics, Clinical Research, Clinical Data Management, Global Drug Safety, Regulatory and Project Management management/staff to meet project ...

Gilead

Director, Biostatistics

Parsippany, NJ

$226K - $292K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

Works collaboratively with Statistical Programming, Biostatistics, Clinical Research, Clinical Data Management, Global Drug Safety, Regulatory and Project Management management/staff to meet project ...

ConnectiveRx

Associate Director, Advanced Analytics

Whippany, NJ · On-site +1

$107K - $160K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Associate Director, Advanced Analytics will manage the people and processes responsible for ... Experience using statistical programming languages such as SAS. * Strong SQL skills with the ...

ConnectiveRx

Associate Director, Advanced Analytics

Whippany, NJ · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Associate Director, Advanced Analytics will manage the people and processes responsible for ... Experience using statistical programming languages such as SAS. * Strong SQL skills with the ...

Gilead

Director, Biostatistics

Parsippany, NJ

$226K - $292K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

The Director, Biostatistics will provide statistical leadership for late-phase Virology clinical ... Partner effectively with Statistical Programming, Clinical Development, Data Management, Clinical ...

Gilead

Director, Biostatistics

Parsippany, NJ

$226K - $292K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

The Director, Biostatistics will provide statistical leadership for late-phase Virology clinical ... Partner effectively with Statistical Programming, Clinical Development, Data Management, Clinical ...

Ameriprise Financial

Director, Workforce Analytics

New York, NY · On-site +1

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

... the Director of Workforce Analytics! In this role, you will have the opportunity to work with ... Experience with statistical programming & modeling (SAS, R, Python, SQL etc.) & data visualization ...

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Showing results 41-60

All JobsStatistical Programming JobsDirector Statistical Programming JobsDirector Statistical Programming Jobs in Passaic, NJ

Director Statistical Programming information

See Passaic, NJ salary details

$158.9K

$290.1K

$356.2K

How much do director statistical programming jobs pay per year?

As of Aug 17, 2026, the average yearly pay for director statistical programming in Passaic, NJ is $290,068.00, according to ZipRecruiter salary data. Most workers in this role earn between $269,700.00 and $333,900.00 per year, depending on experience, location, and employer.

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

To thrive as a Director of Statistical Programming, you need advanced expertise in statistical analysis, programming languages such as SAS or R, and a strong background in clinical trial data, typically supported by a degree in statistics, mathematics, or a related field. Familiarity with regulatory submission processes, CDISC standards, and project management tools is essential, as are relevant certifications like SAS Certified Professional. Leadership, effective communication, and strategic thinking are key soft skills for managing teams and collaborating across departments. These skills ensure high-quality data outputs, regulatory compliance, and successful execution of complex clinical development projects.

What is a director statistical programming?

The job of a director of statistical programming oversees the development and implementation of SAS programs to produce statistical analysis datasets. In this career, your responsibilities include managing the team that generates tables and graphs using the SAS programs for applications such as clinical studies. Other duties include participating in the planning and review of statistical analysis and studying reports, abstracts, and manuscripts as required. You collaborate with project leads to contribute to department operations and standards, such as CDISC for clinical research.

How does a director statistical programming typically collaborate with cross-functional teams in a pharmaceutical or biotech company?

A Director of Statistical Programming regularly works with biostatistics, clinical data management, regulatory affairs, and medical writing teams to ensure that statistical deliverables meet project timelines and regulatory requirements. They coordinate programming efforts across multiple studies, provide leadership and mentorship to programming staff, and help resolve technical or resource-related challenges. Effective collaboration is essential to streamline workflows, maintain data integrity, and ensure clear communication of statistical results within the organization.

What does a director statistical programming do?

A Director of Statistical Programming oversees teams responsible for the programming and analysis of clinical trial data, ensuring the accuracy and integrity of statistical outputs. They set departmental strategies, manage resources, and ensure compliance with regulatory requirements and industry standards. This role also involves collaborating with other departments, such as biostatistics and clinical operations, to support the successful delivery of statistical analyses for drug development and regulatory submissions. They play a key leadership role in mentoring staff and advancing programming processes and technologies.
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Director Statistical Programming jobs near you
Infographic showing various Director Statistical Programming job openings in Passaic, NJ as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, 1% Temporary, and 1% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $290,068 per year, or $139.5 per hour.

Associate Director, Data Operations

Artech Information System LLC

Woodcliff Lake, NJ

Full-time

Re-posted 14 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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