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Associate Director Statistical Programming Jobs in Harrison, NJ

micro1 AI

Director of Biostatistics

Newark, NJ · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

New

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 ...

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 ...

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 ...

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 ...

Cellectis

Senior Director, Biostatistics

Manhattan, NY · On-site

POSITION SUMMARY The Senior Director, Statistics will be in charge of the development and oversight of biostatistics and statistical/clinical programming strategies, operations, and personnel to ...

Cellectis

Senior Director, Biostatistics

Manhattan, NY · On-site

POSITION SUMMARY The Senior Director, Statistics will be in charge of the development and oversight of biostatistics and statistical/clinical programming strategies, operations, and personnel to ...

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Showing results 41-60

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 Aug 7, 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?

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 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 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 August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $293,421 per year, or $141.1 per hour.

Statistical Programmer III

Artech Information System LLC

East Hanover, NJ • On-site

Contractor

Re-posted 22 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

Responsibilities

Coordinate programming activities across several trials with a given compound including publication and regulatory submission activities.

Develop programming specifications for analysis datasets, pooled datasets and deliverables in consultation with the statistician.

Review and provide feedback on statistical analysis plan, output shells, CRF, edit checks and other relevant trial documents.

Develop and comply with project/study programming standards and specifications following internal guidelines

Program according to specifications, analysis datasets, pooled datasets, listings, and figures for clinical trials and submission activities

Support quality control and quality audit of deliverables

Provide input as required at all meetings, discussions and activities covering aspects of Statistical Reporting on trial level activities

Track clinical trial milestones for statistical reporting deliverables.

Maintain records for all assigned projects and archiving of trial/project analysis and associated documentation.

Maintain efficient interfaces with internal and external customers and communicate effectively across line functions.


Skills:

At least 8 years work experience in a Statistical (SAS) programming role preferably supporting clinical trials or in the pharmaceutical industry (5 years for Masters in Mathematics, Statistics/Computer Science or health science graduates).

Advanced knowledge of / experience with SAS and other relevant programming software.

Proven experience in development of advanced MACROs with high programming efficiency; strong programming and problem-solving skills.

Proven experience in leading programmer support for multiple clinical trials and submission activities (or equivalent).

Expertise in programming according to specifications of analysis datasets, pooled datasets, listings, tables and figures for clinical trials and submission activities.

Working knowledge of database design/structures and basic statistics. Working experience in pooling analysis datasets across multiple clinical studies (or equivalent).

Good understanding of global clinical trial/project practices, procedures, methodologies.

Good understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH).

Oncology experience preferred

Strong expertise in CDISC on the submission bucket including CRT programming will be a definite plus.

Intermediate knowledge of office tools

Fluent English (oral and written)

Excellent in people interaction and be a collaborative team player.

Qualifications

MUST HAVE Bachelor or Master's degree in life science, computer science, statistics or equivalent relevant degree.

Additional Information

Regards,

Akriti Gupta

Associate Recruiter(Scientific & Clinical Division)

Artech Information Systems LLC

360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 

Office: 973.967.3409 | Fax: 973.998.2599

Connect with us on - LinkedIn | Facebook | Twitter




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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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