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Director Statistical Programming Jobs in Warren, 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 · On-site

$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

  • 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

$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 ...

Gilead

Director, Biostatistics

Parsippany, NJ · On-site

$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 ...

Otsuka

Associate Director, Real World Data Science

Princeton, NJ · On-site

$61K - $62K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Associate Director of Real-World Data Science is an expert in analysis and methods, providing ... Proficiency in statistical programming (SAS and AWS environment required; R preferred), with ...

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Showing results 41-60

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

Director Statistical Programming information

See Warren, NJ salary details

$158.6K

$289.5K

$355.5K

How much do director statistical programming jobs pay per year?

As of Aug 17, 2026, the average yearly pay for director statistical programming in Warren, NJ is $289,544.00, according to ZipRecruiter salary data. Most workers in this role earn between $269,200.00 and $333,300.00 per year, depending on experience, location, and employer.

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.

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.

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.

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.
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Director Statistical Programming jobs near you
Infographic showing various Director Statistical Programming job openings in Warren, NJ as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $289,544 per year, or $139.2 per hour.

Clinical SAS Programmer

Katalyst Healthcares & Life Sciences

Newark, NJ

Contractor

Re-posted 29 days ago

Job description

Company Description
  • Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
  • We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.
Job Description

Responsibilities:

  • Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s).
  • Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets.
  • Creates and validates tables, figures and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements.
  • Provides input in the design and development of case report forms and clinical databases.
  • Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs.
  • Programs for quality checks for clinical study raw data and report the findings to Data Management.
  • Provides input in the design and development of case report forms and clinical study databases.
  • Reviews or author aCRF, SDTM and ADaM datasets specifications for datasets programming.

Requirements:

  • MS in Statistics, Computer Science, or a related field with at least 3 years or BS in Statistics, Computer Science, or a related field with at least 5 years.
  • Experience in providing statistical programming support to early and late phase clinical trials.
  • Excellent skills in SAS programming and statistical reporting.
  • Knowledge of CDISC standards for SDTM and ADaM and FDA electronic data submission requirements.
  • Familiarity with FDA and ICH regulations and guidelines.
  • Excellent problem-solving skills.
  • Good written and verbal communication skills and organizational and documentation skills.
  • Ability to work on a multidisciplinary team that may include Biostatistics, Medical Directors, Data Management, Medical Writing, Pharmacovigilance, Clinical Operations, Medical Affairs, etc.
  • Ability to prioritize and multi-task effectively.
  • Demonstrated positive attitude and the ability to work well with others.
Additional Information

All your information will be kept confidential according to EEO guidelines.

Katalyst Healthcares & Life Sciences logo

About Katalyst Healthcares & Life Sciences

Sourced by ZipRecruiter

Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

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