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Pharmaceutical Sas Programmer Jobs (NOW HIRING)

Navitas Life Sciences

Senior Statistical Programmer

Background in statistics and statistical analysis is desirable * 10 plus years Pharmaceutical or CRO industry experience in clinical reporting and statistical programming * Strong competence in SAS ...

Crowdstaffing

Biostatistician

Emeryville, CA

PHARMACEUTICAL FDA * SAS * STATISTICAL ANALYSIS * BIOSTATISTICS * Minimum 2 years experience in ... Skilled SAS programming knowledge. * Demonstration of innovation by development or novel ...

Cytel

Senior Statistical Programmer FSP

Cambridge, MA · On-site +1

At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor's degree or equivalent. At least 6 years of related experience with a ...

MMS

Senior Statistical Programmer - Remote

Canton, MI · On-site

We support the pharmaceutical, biotech, and medical device industries with our proven, scientific ... Advanced user in SAS programming, SAS Base, and SAS Macros. * Advanced knowledge of E-Submission ...

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How much do pharmaceutical sas programmer jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for pharmaceutical sas programmer in the United States is $49.00, according to ZipRecruiter salary data. Most workers in this role earn between $34.38 and $61.54 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a pharmaceutical SAS programmer?

To thrive as a Pharmaceutical Sas Programmer, you need strong expertise in SAS programming, clinical data analysis, and a solid understanding of regulatory requirements, typically supported by a degree in statistics, computer science, or a related field. Familiarity with CDISC standards (such as SDTM and ADaM), exposure to clinical trial management systems, and SAS certifications are commonly expected. Attention to detail, problem-solving abilities, and effective communication skills help distinguish top performers in this role. These skills are essential for ensuring the accuracy, compliance, and clarity of clinical trial data submitted to regulatory authorities.

What is a pharmaceutical SAS programmer?

A Pharmaceutical SAS Programmer is responsible for analyzing clinical trial data using SAS software. They develop, validate, and manage programs to generate statistical outputs like tables, listings, and figures for regulatory submissions. Their role ensures compliance with industry standards such as CDISC (SDTM and ADaM) and FDA guidelines. They collaborate with statisticians, data managers, and regulatory teams to ensure accurate data reporting and support drug development processes.

What types of projects or responsibilities can I expect as a pharmaceutical SAS programmer?

As a Pharmaceutical Sas Programmer, you will primarily be tasked with writing and validating programs to analyze clinical trial data, generate tables, listings, and figures (TLFs), and ensure outputs meet regulatory standards. You may collaborate closely with biostatisticians, clinical data managers, and other programmers to interpret datasets, implement statistical analysis plans, and troubleshoot issues in data processing. The work is typically project-based, often requiring you to prioritize multiple studies or phases simultaneously and adhere to tight deadlines. This role offers exposure to the full drug development lifecycle and provides valuable experience for advancing into senior programming, data management, or biostatistics positions.

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Pharmaceutical Sas Programmer jobs near you
Infographic showing various Pharmaceutical Sas Programmer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, 1% Temporary, 4% Contract, and 1% Nights. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $101,929 per year, or $49 per hour.

Job "SAS Statistical Programmer" is shared with you

Navtech, Inc.

Remote

Full-time

Re-posted 10 days ago

Job description

I have an opportunity for "SAS Statistical Programmer" _ (100% REMOTE)" and I am looking for a candidate who can join Immediately if you are interested, reply to me with your updated resume or if you could refer someone I would really appreciate it.
Position : SAS Statistical Programmer
Location : 100% REMOTE
Duration : 6 to 12 Months
ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Independently develops SAS or other programs, and specifications (e.g. SDTM, ADaM), for use in study or other analyses, such as Integrated Safety Summaries.
• May work with clinical data management staff and biostatisticians to address issues in Pinnacle 21 reports, resolve data and programming issues, coordinate and schedule data transfers, and the delivery of required outputs.
• Responsible for programming QC oversight of CRO deliverables such as analysis datasets and tables, listings, and figures (TLFs).
• Independently verifies other programmer's results.
• Adheres to FDA regulations regarding training records, guidelines, and SOPs.
• Adheres to company SOPs and department guidelines.
• Produces study datasets and programs that meet CDISC standards and regulatory requirements.
• Supports ad-hoc requests, as needed.
• Works on multiple tasks at the same time and prioritizes tasks to meet business needs.
• Trouble-shoots technical and project issues.
• Communicates and coordinates with outside departments and/or groups.
Experience:
• Typically requires at least seven years' experience in statistical programming with clinical data and SAS.
• Strong SAS programming skills required, with proficiency in SAS/Base, SAS/Stat and SAS Macros.
• UNIX, S-Plus, R, Tableau, CDISC, and SAS/GRAPH experience are desirable.
• Ability to communicate verbally and in writing in a clear and timely manner.
• Experience in Biotech/Pharmaceutical industry preferred.
SAS Oncology experience is must
Knowledge/Skills/Abilities:
• Has extensive experience in relevant industry/profession and area of specialization.
• Uses professional concepts and company objectives to resolve complex issues in creative and effective ways.
• Identifies and implements methods and procedures to achieve results.
• Leads or manages the work of others by providing guidance to subordinates or teams based on organizational goals and company policy, with responsibility for results, including costs, methods and staffing.
• Must be able to program defensively, check results, and consistently produce accurate output.
• Performs a variety of complicated tasks with a wide degree of creativity and latitude.
• Has complete understanding and wide application of technical principles, theories, concepts and techniques.
• Has good general knowledge of other related disciplines.
• Applies strong analytical and business communication skills.
• Meets timelines on a regular basis.
Regards
Alex Keylor
NAVTECH INC
1600 Golf Road. Suite 1200, Rolling Meadows, IL 60008
Ph: (224) 348-1340 || Email: alex@navtechusa.com || www.navtechusa.com
E-Verified Company
Navtech logo

About Navtech

Sourced by ZipRecruiter

Industry

Civil engineering construction

Company size

11 - 50 Employees

Headquarters location

New Bloomfield, PA, US

Year founded

1996

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