Senior Statistical Programmer

Talentify; Princeton (NJ); Hybrid; USD 96,000 - 110,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) plan

Paid time off

Job summary

Actalent in Princeton, NJ is seeking a Senior Statistical Programmer to provide comprehensive programming support for ongoing studies and submissions. You will create and validate datasets and TLFs, manage vendor oversight, and participate in sponsor reviews of deliverables.

The role requires experience with SDTM/ADaM, FDA/EMA submissions, and CDISC standards, plus collaboration with in-house staff and external vendors to establish global programming standards.

Qualifications

• Eight+ years of statistical programming for clinical trials.
• Expertise in Base SAS, SAS/STAT, SAS/GRAPH, Macro, and SAS 9.2+.
• Experience with CDISC SDTM/ADaM and regulatory submissions.
• Experience with FDA/EMA submissions (CSR support).
• Safety reporting and ISS/ISE data integration across studies.

Responsibilities

• Manage multiple global studies with minimal oversight.
• Oversee vendor programming for SDTM/ADaM and TLFs.
• Collaborate with vendors for analyses and regulatory submissions.
• Review protocols, SAPs, and clinical study reports.
• Support data management with data reconciliation.
• Contribute to department procedures and process improvements.

Skills

Base SAS

SAS/STAT

SAS/GRAPH

Macro

SAS 9.x

CDISC SDTM/ADaM

FDA/EMA submissions

Safety reporting

Data integration

R

Python

Microsoft Office

Education

Master’s Degree in Computer Science/Statistics/Data Science/Health Science

Tools

SAS-LSAF

Job description

Job Title: Senior Statistical ProgrammerJob Description

The Senior Statistical Programmer will provide comprehensive programming support for ongoing studies and submissions. This role involves creating and validating datasets and TLFs, managing vendor oversight, and performing sponsor reviews of deliverables. Additionally, the Senior Statistical Programmer will create patient profiles, provide ad-hoc programming support, represent programming on project study teams, and collaborate with both in-house staff and external vendors to establish and maintain global programming standards.

Responsibilities

• Independently manage and support multiple global studies simultaneously with minimal oversight.
• Oversee programming tasks, including SDTM, ADaM, and TLF preparation performed by vendors, while managing internal statistical programming activities.
• Collaborate with vendors to ensure accurate programming for analysis and regulatory submissions.
• Participate in project teams, review protocols, statistical analysis plans, and clinical study reports.
• Provide programming support to the data management team, including data reconciliation.
• Assist in identifying and maintaining department procedures and contribute to process improvement initiatives.
• Coordinate with Japanese colleagues to align on global programming procedures and standards.
• Assist in regulatory submissions and support responses to regulatory authority requests.
• Provide expertise in FDA/EMA guidances related to electronic format submissions.
• Ensure compliance with ICH/GCP guidelines and CDISC standards for data structures and validation.

Essential Skills

• Minimum eight years of extensive experience in statistical programming for clinical trials in the pharmaceutical or life sciences industry.
• Expertise in Base SAS, SAS/STAT, SAS/GRAPH, Reporting and Graphical Procedures, Macro, and SAS Version 9.2 or higher.
• Experience with CDISC SDTM/ADaM standards and regulatory submission requirements.
• Proficiency in FDA/EMA regulatory submissions, including CSR support.
• Experience in safety reporting and data integration for ISS/ISE across multiple studies.

Additional Skills & Qualifications

• Master’s Degree in Computer Science, Data Science, Health Science, Statistics, or a related discipline.
• Preferred experience with R and/or Python.
• Experience with SAS-LSAF (Life Science Analytics Framework) is preferred.
• Strong proficiency in Microsoft Office applications.
• Ability to organize, prioritize, meet deadlines, and work in a dynamic environment.
• Strong interpersonal and communication skills.
• Cultural sensitivity and ability to develop consensus within a multinational organization.

Work Environment

This position requires working in the office at least two days a week. The company is a leading global specialty pharmaceutical and biotechnology entity with headquarters in Tokyo, Japan, and is expanding its global presence with a new U.S. manufacturing site in North Carolina. The work environment supports innovation in biologics and gene- and cell-based therapies, emphasizing patient-focused advancements and strategic partnerships. The organization values a collaborative culture and offers opportunities for international travel.

Job Type & Location

This is a Contract position based out of Princeton, NJ.

Pay and Benefits

The pay range for this position is $70.00 - $80.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a hybrid position in Princeton,NJ.

Application Deadline

This position is anticipated to close on Sep 14, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [e-mail] for other accommodation options.

San Francisco Fair Chance Ordinance:

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector:

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.