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Temporary Sas Contractor Jobs (NOW HIRING)

Penumbra

Manager, Statistical Programming

... contractors, temps, CRO, consultants). * • Oversee team effort related to derive data sets and ... Oversee the development of new SAS Macros. * • Manage CROs and other outside vendors for ...

WellSense Health Plan

Quality Performance Strategist

$121K - $156K/yr

... based staff, contractors, and temporary employees, no direct FTE management responsibility ... Experience Preferred/Desirable: · Knowledge and experience in SQL, SAS, and/or other database ...

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As of Jul 21, 2026, the average hourly pay for temporary sas contractor 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.
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Infographic showing various Temporary Sas Contractor job openings in the United States as of July 2026, with employment types broken down into 1% Locum Tenens, 74% Full Time, 7% Part Time, and 18% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $101,929 per year, or $49 per hour.

SAS Programmer II / Clinical Trials / Remote Work

Pioneer Data

West Chester, PA • On-site

Contractor

Re-posted yesterday

Job description

Position Details:
Our client, a world-leading Pharmaceutical Company in Memphis, TN is currently looking for a SAS Programmer II to join their expanding team.
Job Title: SAS Programmer II / Clinical Trials / Remote Work
Duration: 21 months contract, extendable up to 24 Months
Location: Remote Worker
Client Location: Memphis, TN

Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
 
Job Description:
Title: Clinical Programming – Contractor – Analysis and Reporting (ADaM)
Shift Schedule:
Regular 40 week working schedule (morning)
Duration:
Up to 2 year assignment
Temp to Perm:
Not during this time
Core Essential Skill Sets:
1. Bachelors + 5 year, Masters + 4 years of professional experience in a pharmaceutical or clinical research setting as a programmer
2. Proficient knowledge of clinical trials and drug development process, industry standards, statistical concepts used in analysis and submissions of clinical trial data.
Position Summary:
The Clinical Programming (Contractor) is responsible for providing comprehensive programming support, including managing the timely and accurate execution of programming components of clinical trials.
The clinical programming contractor independently manages completed projects that involve global tasks, or cross functional teams
The role may require providing inputs to design and analysis, and reporting the results of clinical trials, including programming rules and mocked T/L/G. In addition, providing programming support for publication for our marketed drugs.
Travel Requirements:
N/A
Essential Duties & Responsibilities:
1. Primarily works at the Study, product / program level
2. Provides comprehensive programming support, including development of programs, ADaM specifications, analysis (datasets, TLFs) complying with regulatory requirements, departmental SOPs and work practices.
3. Manages and Delivers assignments with good quality and within timelines
4. Provides programming support to CDISC based e-submission. Develop, debug, and enhance SAS programs to support quality control of safety or efficacy derived datasets and TLFs.
5. Implement programming standards and comply with regulatory requirements among project team members and across all projects; communicate to management on project status and resource gaps.
6. Responsible for the standardization of GSD deliverables (TLGs, Datasets) across study projects within an indication/therapeutic area. Provides input on opportunities for process improvement
7. Proactively communicates issues impacting programming deliverables with Stat or DM team members.
Position Requirements:
Education Required:
Bachelor’s Degree/Master’s Degree in Science, Statistics, Information Technology or equivalent combination of education and related work experience.

Experience Required:
Bachelors + 5 year, Masters + 4 years of professional experience in a pharmaceutical or clinical research setting as a programmer.
Proficient knowledge of clinical trials and drug development process, industry standards, statistical concepts used in analysis and submissions of clinical trial data.
Strong understanding of SDTM, ADaM standards and Implementation guides.
Demonstrated proficiency in using SAS to produce analysis datasets, TLFs, eSUB components and using other software applications (eg. Pinnacle 21, XML and MS Office)
Demonstrated ability to work independently and in a team environment.
 
Experience Preferred:
Specialized or Technical Knowledge Licenses, Certifications needed:
Functional Knowledge: Expert level of programming skills and problem resolution in SAS.
Expert level of knowledge in CDISC based e-submission (creation of ADaM datasets and associated TLGs in study/project (e.g. ISS/ISE), creation of Bioresearch Monitoring (BIMO) Inspections).
Have solid knowledge of statistical models used for efficacy data analysis.
Company/Industry Related Knowledge: Advanced knowledge of government regulations (such as CDISC and ICH) pertaining to drug development in multiple therapeutic areas.
Job-Specific Competencies:
1. Tackles difficult problems; identifies solutions and recommends action management
2. Influences communication toward common understanding and actionable results;
3. Good oral and written communication skills.