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Contract Pharmaceutical Sas Programmer Jobs (NOW HIRING)

BCforward

SAS Developer

Charlotte, NC · On-site

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

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 ...

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 · On-site

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 ...

WorkNovas LLC

Sr. Cobol Developer

Cincinnati, OH · On-site

$48.25 - $65.25/hr

Cincinnati Ohio 45227 Contract 5 Days Onsite Skills: Base SAS Programmer, CICS COBOL, COBOL, Dev, QA, File Transfer Protocol (FTP), IBM MVS Z/OS, JCL, Platform Engineering - Mainframe and Wealth ...

Tanisha Systems

SAS CI

New York, NY · On-site

Contract Mandatory Skills : • Strong experience in building Campaigns on SAS CI • Strong experience on SAS Visual Analytics and Campaign Performance reports • Good understanding of overall ...

Tanisha Systems

SAS CI

New York, NY · On-site

Contract Mandatory Skills : Strong experience in building Campaigns on SAS CI Strong experience on SAS Visual Analytics and Campaign Performance reports Good understanding of overall marketing ...

Crowdstaffing

Biostatistician

Emeryville, CA · On-site

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 ...

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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 Sep 4, 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 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 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.

Are Contract Pharmaceutical SAS programmers in demand?

Contract Pharmaceutical SAS programmers are in steady demand due to the ongoing need for data analysis and reporting in the pharmaceutical industry. Skills in SAS programming, clinical trial data management, and regulatory compliance increase employability, especially for contract roles that offer flexibility and specialized expertise.

How much do contract pharmaceutical SAS programmers make?

Contract pharmaceutical SAS programmers typically earn between $50 and $100 per hour, depending on experience, location, and project complexity. Senior programmers with specialized skills or certifications can command higher rates, especially for short-term or high-demand projects.

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

Data Standard Analyst - Biostatistics Team

Medpace, Inc.

Cincinnati, OH • On-site, Remote

Full-time

Medical, Retirement, PTO

Re-posted 4 days ago

Key responsibilities

  • Implement edit check specifications via SAS programming to assist with reconciliation of data discrepancies.

  • Create annotated CRFs and mapping specifications per CDISC SDTM standards and generate SDTM data by implementing data standards for collected study data.

  • Perform validation of CDISC SDTM data in accordance with SOPs and guidance documents, ensuring data conforms to regulatory standards.

Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

15th of 75 rated research

Job description

Job Summary

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Data Standard Analyst to join our Biostatistics team. This position will work on a team to accomplish tasks and projects that are instrumental to the company's success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities
  • Implement edit check specifications via SAS programming to assist with reconciliation of data discrepancies;
  • Create annotated CRFs and mapping specifications per CDISC SDTM standards;
  • Create SDTM data via SAS programming by implementing data standards for collected study level source data;
  • Perform validation of CDISC SDTM data in accordance with SOPs and guidance documents;
  • Ensure SDTM data conforms to the data standards expected by regulatory agencies;
  • Assist with creation of the define package for submission to regulatory agencies;                              
Qualifications
  • Bachelor's Degree in Math, Statistics, Life Sciences, or equivalent
  • SAS programming knowledge preferred

TRAVEL: None

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events and intramural sports

Cincinnati Headquarters Experience

    • A modern corporate campus designed to support collaboration and productivity
    • Multiple on-site dining options in the heart of Madison Square
    • Free on-site parking
    • Convenient access to on-site 24-7 fitness and wellness facilities

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

Employment Type: OTHER

What Medpace employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

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About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992

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