ZipRecruiter

Log In

1

Associate Statistical Programmer Jobs in New Jersey

MSD

Associate Director, Biostatistics

Rahway, NJ · On-site

Purpose of the Role The Associate Director Biostatistics will lead and oversee the planning and ... Proficiency in statistical programming languages such as SAS or R and familiarity with advanced ...

next page

Showing results 1-20

All JobsAssociate Statistical Programmer JobsAssociate Statistical Programmer Jobs in New Jersey

Associate Statistical Programmer information

See New Jersey salary details

$85.8K

$149.5K

$252.8K

How much do associate statistical programmer jobs pay per year?

As of Jul 19, 2026, the average yearly pay for associate statistical programmer in New Jersey is $149,536.00, according to ZipRecruiter salary data. Most workers in this role earn between $126,900.00 and $162,400.00 per year, depending on experience, location, and employer.

What is an Associate Statistical Programmer?

An Associate Statistical Programmer is an entry-level professional who assists in the programming and analysis of clinical trial data, primarily within the pharmaceutical or biotechnology industries. They use statistical software, such as SAS or R, to create, validate, and maintain datasets, tables, listings, and figures required for clinical study reports. Their work supports biostatisticians and clinical teams in ensuring data accuracy and regulatory compliance. This role is ideal for those with a background in statistics, mathematics, or computer science, looking to start a career in clinical data analysis.

How does an Associate Statistical Programmer typically collaborate with biostatisticians and data managers in clinical research projects?

As an Associate Statistical Programmer, you will frequently collaborate with biostatisticians to understand statistical analysis plans and translate them into clear programming specifications. You’ll also work closely with data managers to ensure data integrity and resolve any data discrepancies before analysis. Effective communication and teamwork are essential, as you’ll often participate in project meetings, provide programming support, and help deliver high-quality datasets and reports under tight timelines. This collaborative environment is key to ensuring accurate and timely clinical trial results.

What is the difference between Associate Statistical Programmer vs Statistical Programmer?

AspectAssociate Statistical ProgrammerStatistical Programmer
Required CredentialsBachelor's degree in statistics, mathematics, or related field; some roles may require basic programming skillsBachelor's or master's degree; more experience in programming and statistical analysis
Work EnvironmentEntry-level, supporting senior programmers; often in clinical research or pharmaceutical companiesMore independent, handling complex analyses; similar industry settings
Employer & Industry UsageCommon in clinical trials, pharmaceutical, and biotech companiesUsed across similar industries, often as a step up from associate roles

The main difference between an Associate Statistical Programmer and a Statistical Programmer lies in experience and responsibility level. Associate roles are typically entry-level, focusing on supporting tasks under supervision, while Statistical Programmers handle more complex analyses independently. Both roles are vital in clinical research and biotech industries, with the associate position serving as a stepping stone to more advanced programming roles.

What are the key skills and qualifications needed to thrive as an Associate Statistical Programmer, and why are they important?

To thrive as an Associate Statistical Programmer, you need a solid background in statistics, programming (especially SAS or R), and familiarity with clinical trial data, typically supported by a degree in statistics, mathematics, or a related field. Proficiency with statistical software (such as SAS, R, or Python), CDISC standards, and data management tools is essential, and certifications in SAS programming can be advantageous. Attention to detail, strong problem-solving abilities, and effective communication skills help you collaborate with clinical teams and ensure data quality. These skills and qualities are vital for delivering accurate statistical analyses that support regulatory submissions and evidence-based decision-making in clinical research.
What are the most commonly searched types of Statistical Programmer jobs in New Jersey? The most popular types of Statistical Programmer jobs in New Jersey are:
What are popular job titles related to Associate Statistical Programmer jobs in New Jersey? For Associate Statistical Programmer jobs in New Jersey, the most frequently searched job titles are:
What job categories do people searching Associate Statistical Programmer jobs in New Jersey look for? The top searched job categories for Associate Statistical Programmer jobs in New Jersey are:
What cities in New Jersey are hiring for Associate Statistical Programmer jobs? Cities in New Jersey with the most Associate Statistical Programmer job openings:
Associate Statistical Programmer jobs near you
Statistical Programmer III

Statistical Programmer III

Artech Information System LLC

East Hanover, NJ

Contractor

Re-posted 2 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




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

View All Artech Jobs

Apply