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Entry Level Clinical Sas Programmer Jobs (NOW HIRING)

PSI CRO

Principal Statistician

Durham, NC

Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research * Expert knowledge and understanding of the SAS programming * Expert ...

IQVIA, Inc.

Mgr, Database Management Systems

Durham, NC · On-site

$84K - $211K/yr

This role will serve as a subject matter expert in clinical data standards, Medidata Rave global library development, and SAS programming, partnering with cross-functional teams to ensure high ...

Pioneer Data

Biostatistician

Raritan, NJ · On-site

Biostatistician / Clinical Data Detailed Description: * Responsible for statistical aspects of ... Work with SAS programmers as part of a biostatistics team. * Knowledge of applied parametric and ...

Hadronts

Entry Level Software Developer

Austin, TX

... Entry Level Software Developer Job Duties & Responsibilities Do you enjoy programming and ... The tools we routinely use include SAS, SQL Server, SSRS, Visual Studio .NET, and C#. As one of our ...

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Entry Level Clinical Sas Programmer information

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How much do entry level clinical sas programmer jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for entry level clinical sas programmer in the United States is $54.04, according to ZipRecruiter salary data. Most workers in this role earn between $41.59 and $68.03 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Entry Level Clinical Sas Programmer position, and why are they important?

To thrive as an Entry Level Clinical SAS Programmer, you need a solid understanding of SAS programming, statistics, and clinical trial processes, often supported by a degree in computer science, statistics, or a related field. Familiarity with SAS software, data management systems, and FDA or CDISC standards is highly valued, and SAS certification can be a plus. Attention to detail, strong problem-solving skills, and effective communication are key soft skills for this role. These competencies ensure high-quality data analysis, regulatory compliance, and clear collaboration across teams in pharmaceutical or clinical research settings.

What is an Entry Level Clinical SAS Programmer job?

An Entry Level Clinical SAS Programmer is responsible for programming and analyzing clinical trial data using SAS software. They assist in creating datasets, reports, and statistical outputs that comply with regulatory standards. Their work supports biostatisticians and clinical teams in pharmaceutical companies, contract research organizations (CROs), or healthcare institutions. This role requires knowledge of SAS programming, clinical research processes, and regulatory requirements such as CDISC standards. It is an excellent starting point for those looking to build a career in clinical data analysis and biostatistics.

What are some typical responsibilities of an Entry Level Clinical SAS Programmer in a clinical research setting?

Entry Level Clinical SAS Programmers are primarily responsible for writing and validating SAS code to process clinical trial data, generate tables, listings, and figures, and support statistical analysis plans. They work closely with biostatisticians, data managers, and other team members to ensure data integrity and compliance with regulatory standards. Daily tasks may involve data cleaning, programming data checks, and documenting code for reproducibility. This role offers great exposure to the clinical data lifecycle and provides a strong foundation for professional growth within clinical research and data analytics.

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Entry Level Clinical Sas Programmer jobs near you
Infographic showing various Entry Level Clinical Sas Programmer job openings in the United States as of July 2026, with employment types broken down into 3% As Needed, 72% Full Time, 18% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $112,399 per year, or $54 per hour.

Principal Statistician

PSI CRO

Durham, NC

Full-time

Re-posted 7 days ago

Job description

Company Description

We are the company that cares - for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

You will contribute to statistical activities related to global clinical trials and work closely with international teams of statisticians, programmers and data managers, including the role of biostatistics project lead.

In this role, you will:

  • Act as a communication line for project teams, clients, vendors and internal team on statistical questions
  • Conduct statistical analysis for clinical trials including, interim analysis, final analysis, analysis for DSMBs/DMCs and PK analysis
  • Develop and review study protocols, statistical analysis plans, analysis dataset specifications according to CDISC ADaM standard and other project-specific documents
  • Review statistical deliverables such as tables, figures, listings and analysis datasets
  • Conduct departmental induction course and project-specific training for statisticians and SAS programmers
  • Prepare for and attend internal and external study audits pertinent to Statistics
  • Participate in preparation of internal/external audits follow up
  • Provide input to standard operating procedures and other Quality Systems Documents (QSDs) pertinent to activities of Biostatistics department
  • Liaise with DM on statistical questions related to data issues
  • Participate in bid defense and in kick-off meetings
  • Lead teams of SAS programmers and/or statisticians on the project level
Qualifications
  • MSc in Statistics or equivalent
  • Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research
  • Expert knowledge and understanding of the SAS programming
  • Expert knowledge and understanding of CDISC ADaM standard
  • Expert knowledge and understanding of adaptive designs
  • Expert knowledge and understanding of sample size calculation
  • Expert knowledge and understanding of relevant regulations and guidelines (e.g. FDA, EMA, ICH)
  • Ability to apply advanced statistical techniques in support of clinical research studies and to analyze, interpret, and draw conclusions from complex statistical information
  • Ability to consult with clinical investigators, interpret research requirements, and determine statistical analysis strategies
  • Strong presentation and communication skills
Additional Information

Our mission is to be the best CRO in the world as measured by our employees, clients, sites, and vendors. Our recruitment process is easy and straightforward, and we'll be there with you every step of the way. 

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