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No Experience Sas Programmer Jobs (NOW HIRING)

Medpace

SAS Programmer - Entry Level

Cincinnati, OH · On-site

SAS Programming experience required * Minimum 3.4 GPA Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to ...

Integrated Resources INC

SAS Programming

Madison, NJ

Acts as primary programmer to produce tables, listings, and figures for the clinical study report ... No OT, No Travel required. All work to be performed onsite in Madison. Qualifications Graduated ...

Atorus Research

Sr R & SAS Programmer

Chesterbrook, PA · On-site

Sr SAS & R Programmer onsite in the Chesterbrook, PA area 3 days/week SUMMARY The contract Senior ... Ability to communicate details of the analysis to other team members with less technical experience.

DLH

Programmer Analyst (SAS or R) (Job 1366)

$50K - $80K/yr

Overview DLH Corp, is looking for a Public Health Programmer Analyst , using SAS or R ,to join our ... Strong, demonstrated experience with SAS. * Familiarity with R coding. * Clear communication ...

DLH

OR · On-site

$50K - $80K/yr

Overview DLH Corp, is looking for a Public Health Programmer Analyst , using SAS or R , to join our ... Strong, demonstrated experience with SAS. * Familiarity with R coding. * Clear communication ...

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How much do no experience sas programmer jobs pay per hour?

As of Jun 25, 2026, the average hourly pay for no experience 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 in the No Experience Sas Programmer position, and why are they important?

To thrive as a No Experience SAS Programmer, foundational knowledge of programming logic, basic statistics, and a willingness to learn are essential, often paired with a relevant bachelor's degree. Familiarity with the SAS software suite, introductory certifications (like SAS Base Programming), and spreadsheet tools such as Excel are commonly expected. Strong problem-solving skills, attention to detail, and effective communication help you collaborate with team members and interpret data requirements. These skills enable new programmers to quickly adapt, produce accurate analyses, and grow into more complex SAS programming roles.

What is a No Experience Sas Programmer job?

A No Experience SAS Programmer job is an entry-level role for individuals with little to no prior work experience in SAS programming. These positions are typically offered by companies willing to train candidates in data management, statistical analysis, and reporting using SAS software. Employers may look for candidates with a background in statistics, mathematics, or computer science and a willingness to learn. Responsibilities often include writing simple SQL queries, cleaning datasets, and generating basic reports. Strong analytical skills and attention to detail are important for success in this role.

What are some common challenges faced by entry-level SAS Programmers with no prior experience?

Entry-level SAS Programmers with no prior experience often face challenges such as adapting to complex data structures, learning to efficiently write and debug code, and understanding industry-specific datasets. You may also need time to become comfortable working with large volumes of data and collaborating with cross-functional teams in fields like healthcare, finance, or research. However, companies typically provide training and mentorship to help you transition smoothly. Proactively asking questions and seeking feedback can accelerate your learning and help you build confidence in your daily responsibilities.

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No Experience SAS Programmer jobs near you
Sr. SAS Programmer

Sr. SAS Programmer

Katalyst HealthCares & Life Sciences

Worcester, MA • On-site

Other

Posted yesterday

Job description

Biostatistics Team Support

Responsibilities:

To support the Biostatistics team by carrying out programming activities of statistical programmers and overseeing external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical studies and publications.

Contributes to the overall efficiency and best practice of the Biostatistics group, demonstrating the ability to work efficiently and to a high standard within a clinical team environment.

Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming activities among the study programmers to achieve timely progress in the following areas: SDTM datasets, ADaM datasets, statistical tables, figures, listings, and other internal and external requests (e.g., publications).

Accessing and converting data to SAS from Database management system and PC file formats (e.g., MS Excel, text files).

Working with external vendors in order to develop or monitor the content and structure of SAS data sets.

Working closely with clinicians, statistician, and publication managers to generate and QC outputs for publications; review publication (abstract/manuscripts) to ensure accuracy, quality and soundness of statistical methodologies; coordinate internal resource utilization for publication and generate activities metrics for management review.

Providing input to the Database and CRF Development, creating edit check programs and providing feedback to the Data Management.

Providing input in developing statistical analysis plans, specifications of analysis datasets, validation plans, and other related documents.

Maintaining standards for programming activities.

Working independently to accomplish tasks and goals defined by supervisor.

Bringing in new ideas to improve the programming process.

Requirements:

Minimum of bachelor's degree in related science discipline.

Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment.

Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office.

Experience in CDISC data standards, e.g SDTM and ADaM.

Proven experience with Unix and Windows operating systems.

Understanding of the software development life cycle.

Understanding of FDA guidelines.

Good organization, time management and attention to detail skills needed to work in a stressful environment under tight deadlines while maintaining focus on details and quality.

Applies good judgment and demonstrates initiative to resolve issues.

Strong verbal, written and interpersonal communication skills needed to work effectively in a team environment.

Katalyst Healthcares & Life Sciences logo

About Katalyst Healthcares & Life Sciences

Sourced by ZipRecruiter

Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

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