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Contract Pharmaceutical Sas Programmer Jobs (NOW HIRING)

CICONIX, LLC

SAS Programmer

Fort Detrick, MD · On-site

  • Medical

  • Retirement

  • PTO

SAS Programmer About CICONIX: CICONIX LLC is a Veteran Owned Small Business specializing in ... TBD . *This position is contingent and will begin upon contract award. CICONIX LLC is an Equal ...

Veredus - DC

Jr. Data Anaylst (SAS)

Alexandria, VA

$22/hr

Company Description Jr. SAS Programmer Location: Alexandria, VA One year long contract Pay rate: up to $22/ hour Interview process: phone, F2F Must be US citizen, able to get a public trust Why the ...

TechData Service Company LLC

Be Seen First

Clinical Statistical Programming Infrastructure Engineer (SAS/AWS)- BB

Boston, MA · Remote

$70 - $130/hr

  • Medical

  • Dental

  • Vision

  • PTO

SAS programming experience in biotechnology, pharmaceutical, or clinical research environments. * Strong knowledge of Base SAS, SAS Macro programming, and utility macro development. * Experience ...

Lorven Technologies

SAS Developer

Job Title: SAS Developer Location: Remote Hiring Type: Contract & Full-Time Required Skills: SAS, SQL, SAS ETL and SAS VIYA, PROC CAS, PROC CASUTIL Preferred Skills: Docker/Kubernetes ...

BCforward

SAS Developer

Charlotte, NC

Charlotte, NC Contract length: 08+ Months Experience in building automated Production environment on SAS Grid SAS Advanced certified must Financial institution experience required. - 7+ years ...

Saxon Global

SAS Developer

Charlotte, NC · On-site

SAS Developer Duration: 18 + Months Contract City : Charlotte, NC Interview:Phone And Skype Day to Day Responsibilities? Hands-on development experience using SAS. They will be supporting the re ...

Tech Tammina

SAS Analyst

Orlando, FL · On-site

W2 contract Looking for SAS Analyst in Orlando, Florida. This position will report directly to the ... Background in SAS programming is paramount to success in this role, as well as a complete ...

Atria Group LLC

SAS Developer/Analyst

Addison, TX

Requirement: 1. Apply and demonstrate expertise with efficient DATA step, SQL programming and SAS ... Typically a long-term (12-18+ month) contract. * Candidates need to be able to interview on site in ...

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 ...

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All JobsContract Pharmaceutical Sas Programmer Jobs

Contract Pharmaceutical Sas Programmer information

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$14

$49

$79

How much do contract pharmaceutical sas programmer jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for contract 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 is the difference between Contract Pharmaceutical Sas Programmer vs Contract Clinical SAS Programmer?

AspectContract Pharmaceutical SAS ProgrammerContract Clinical SAS Programmer
CertificationsTypically requires SAS certifications, pharmaceutical industry knowledgeRequires SAS certifications, clinical trial experience
Work EnvironmentPharmaceutical companies, biotech firms, CROs in drug developmentClinical research organizations, hospitals, CROs in clinical trials
Employer & Industry UsagePrimarily in pharmaceutical and biotech sectorsPrimarily in clinical research and trial management

Contract Pharmaceutical SAS Programmers focus on data analysis and reporting within pharmaceutical companies, while Contract Clinical SAS Programmers work mainly on clinical trial data across various research organizations. Both roles require SAS expertise and industry-specific knowledge, but their primary focus and work environment differ slightly.

What is a contract pharmaceutical SAS programmer?

A Contract Pharmaceutical SAS Programmer is a professional who works on a contract basis to manage and analyze clinical trial data using SAS (Statistical Analysis System) software for pharmaceutical companies. Their primary responsibilities include programming, validating, and generating statistical reports that support drug development and regulatory submissions. They collaborate with statisticians, data managers, and clinical teams to ensure data integrity and compliance with industry standards such as CDISC. Contract programmers may work independently or through staffing agencies, often on multiple projects for different clients.

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

To thrive as a Contract Pharmaceutical SAS Programmer, you need strong programming skills in SAS, knowledge of clinical trial data, and a background in statistics or life sciences, usually supported by a relevant degree. Familiarity with CDISC standards (SDTM, ADaM), clinical data management systems, and experience with regulatory submission processes are highly valued. Attention to detail, problem-solving ability, and effective communication with cross-functional teams distinguish top performers in this role. These skills ensure accurate data analysis, compliance with industry standards, and successful collaboration in delivering reliable results for clinical studies.

What are some common challenges faced by contract pharmaceutical SAS programmers when working with multiple clinical trial projects simultaneously?

Contract Pharmaceutical SAS Programmers often juggle several clinical trial projects at once, which can present challenges such as managing tight timelines, adapting to varying data standards, and coordinating with multiple study teams. Effective communication and strong organizational skills are essential to ensure data quality and timely delivery. Additionally, contractors must quickly familiarize themselves with each sponsor’s unique processes and regulatory requirements, making flexibility and adaptability key to success in this role.

What cities are hiring for Contract Pharmaceutical Sas Programmer jobs?

Cities with the most Contract Pharmaceutical Sas Programmer job openings:

What are the most commonly searched types of Pharmaceutical Sas Programmer jobs?

The most popular types of Pharmaceutical Sas Programmer jobs are:

What states have the most Contract Pharmaceutical Sas Programmer jobs?

States with the most job openings for Contract Pharmaceutical Sas Programmer jobs include:

Contract Pharmaceutical Sas Programmer jobs near you

SAS Programmer II / Clinical Trials / Remote Work

Pioneer Data

West Chester, PA • On-site

Contractor

Re-posted 25 days ago

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.