Job description:-

We are seeking a skilled Clinical SAS Programmer with expertise in SDTM, ADaM (Safety and Efficacy) , and TLFs to join our team. The ideal candidate must also have hands-on experience or knowledge of R programming.

Location: Ridgefield, CT, United States
Job Type: [Full-Time & Contract]

Key Responsibilities::
• Develop and validate SDTM and ADaM datasets following CDISC standards.
• Generate Tables, Listings, and Figures (TLFs) for clinical study reports.
• Perform statistical programming for clinical trials in SAS and R.
• Work closely with statisticians, data managers, and clinical teams to ensure data integrity and compliance.
• Develop macros and automate processes to optimize programming efficiency.
• Ensure compliance with GCP, CDISC, and FDA submission requirements.

Required Qualifications::
• 3+ years of experience in clinical SAS programming.
• Strong expertise in SDTM, ADaM, and TLFs.
• Hands-on experience or knowledge of R programming.
• Familiarity with CDISC standards, FDA/ICH guidelines, and submission requirements.
• Strong analytical and problem-solving skills.
• Excellent communication and teamwork abilities.

Preferred Qualifications: • Experience with Shiny, ggplot2, or other R packages for visualization and reporting.
• Exposure to machine learning or statistical modeling in R.
• Prior experience in pharmaceutical, biotech, or CRO environments.

How to Apply:

If you meet the above qualifications and are interested in joining our team, please send your resume to pc_mentriix@hscrp.net.