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# Junior Clinical SAS Programmer

- **Company:** Guru Schools
- **Location:** Charlotte, NC, United States (Remote available)
- **Experience:** Starter
- **Contract:** Permanent contract
- **Skills:** Data Analysis, Clinical Data Management, Computer Programming, Coherent Remote File System (CRFS), Data Validation, Data Cleansing, SAS (Software), SQL Databases, Macros, Information Technology
- **Published:** August 3, 2026
- **Apply:** https://www.careerjet.com/jobad/us9ead61750430a77c66c8a48c9350d4d3

## About the Role

We are seeking motivated recent graduates and early-career professionals with 0-2 years of experience who are interested in building a career in Clinical SAS Programming. This opportunity is ideal for candidates passionate about clinical research, data analysis, and programming in the pharmaceutical, biotechnology, and healthcare industries.
We provide comprehensive Clinical SAS training, real-time project exposure, interview preparation, resume assistance, and continuous career support to help you establish a successful career., * Bachelor's or Master's degree in Life Sciences, Pharmacy, Biotechnology, Computer Science, Statistics, or a related field.

 * 0-2 years of experience or academic/project exposure in Clinical SAS Programming.
 * Basic knowledge of Base SAS, SAS Macros, and SQL.
 * Understanding of CDISC standards (SDTM, ADaM) and clinical trial processes.
 * Familiarity with clinical research concepts, GCP, and FDA regulatory guidelines is a plus.
 * Strong analytical, problem-solving, and communication skills.
 * Ability to work independently as well as collaboratively in a team environment.

## Description

* Develop, validate, and maintain SAS programs for clinical trial data analysis and reporting.
 * Generate SDTM, ADaM, and TLFs (Tables, Listings, and Figures) according to CDISC standards.
 * Perform data validation, quality checks, and reconciliation to ensure data accuracy.
 * Work with clinical data management and biostatistics teams to support clinical study deliverables.
 * Review study protocols, Statistical Analysis Plans (SAPs), and CRFs to understand study requirements.
 * Support data cleaning activities and resolve data discrepancies.
 * Create and maintain programming documentation following regulatory guidelines.
 * Collaborate with cross-functional teams to ensure timely and accurate clinical study submissions., * Remote Work from Home
 * Structured Clinical SAS Training
 * Real-Time Project Experience
 * Resume Preparation & Mock Interviews
 * Career Guidance and Placement Support
 * Continuous Learning and Professional Development


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