Average salary: $131,066 /yearly
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- ...PEGUS Research in Salt Lake City, UT invites a Statistician/SAS Programmer to join our analytics team. You will perform statistical analyses, generate tables and figures, and prepare data for FDA submissions in a fast-paced, remote-friendly environment. The role requires...SASRemote work
- ...Detail-oriented and motivated, the full-time salaried Statistician SAS Programmer will conduct statistical analysis, validate data for FDA submissions, and develop statistical programs in a remote work environment. Key responsibilities Conduct statistical analysis by...SASFull timeRemote work
- ...Job Description Job Description Description: SAS Programmer Location: Remote/Hybrid Job Type: Full-Time Position Overview: Venesco is seeking a skilled SAS Programmer to support clinical data analysis and regulatory submission activities. Requirements...SASFull timeRemote work
- ...Collabera is seeking an experienced Statistical Programmer to support clinical trial safety and efficacy analyses with hands-on SAS programming and ADaM dataset development. Strong CDISC ADaM/SDTM knowledge and ability to interpret study documentation are essential for...SASRemote work
C++ Storage Developer/C++ with Storage/Embedded Engineer/NVMe Storage Engineer/Embedded/Storage- Emb
...NVMe Storage Protocols \n Low-Level Programming \n SSD/HDD/Cloud Storage Internals \n \n Preferred Skills \n \n SATA, SAS, RAID, and File Systems \n Storage Performance Tuning \n Tool Development \n Windows and Linux Platforms \n SQL \n PowerShell...SASFull timeRemote work- ...submissions. The position is fully remote and can sit anywhere in the US. Ideal candidates have 5+ years in statistical programming, strong SAS skills, and familiarity with CDISC standards. The job emphasizes collaboration across clinical programs, data management, and...SASRemote work
- Job SummaryOur corporate activities are growing rapidly, and we are currently seeking a full-time, office-based SAS Programmer 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...SASFull timeContract workWork at officeWork from home
- ...Programmer for a 6-month contract that is fully remote within the United States. The role offers a $70/hr W2 arrangement and requires strong SAS programming skills to develop, validate, and document ADaM datasets and tables for CSR deliverables. You will work on SDTM/ADaM...SASContract workRemote work
- ...quality while mentoring junior programmers. The role is fully remote for US-based projects with international collaboration across Europe. Strong SAS/CDISC expertise and leadership experience are required to manage submissions and review complex outputs. #J-18808-Ljbffr...SASRemote work
- ...timelines for statistical data analysis and reporting. This remote, full-time role requires expert CDISC (SDTM/ADaM) knowledge, strong SAS programming skills, and the ability to develop robust macros and scripts for study outputs, listings, and regulatory submissions. #J-...SASFull timeRemote work
- ...Job Description Job Description Job Summary: We are seeking an experienced Real World Evidence (RWE) Programmer with strong SAS, SQL, and R programming expertise to support observational research and healthcare data analytics initiatives for pharmaceutical and...SASRemote work
$106k - $170.2k
...as PMA or 510(k) submissions), and continual learning in a regulated environment. Essential Job Functions • Develop and validate SAS programs to generate analysis datasets, tables, listings, and figures (TLFs) that support clinical trial reporting, regulatory...SASInterim roleInternshipLocal areaImmediate startRemote work$186k
...position requires an advanced degree in statistics, 15+ years of experience in clinical trial design, and strong programming skills in SAS and R. You will play a crucial role in ensuring effective communication with stakeholders, developing innovative trial designs, and...SASRemote work- ...seeking an Associate Director of Statistical Programming to lead programming efforts in oncology trials. This role includes hands-on SAS programming and the oversight of CRO statistical programmers, as well as ensuring compliance with CDISC standards. The ideal candidate...SASRemote work
- ...Statistics or Biostatistics, with substantial experience in clinical trial design and analysis. The SLS will collaborate closely with cross-functional teams to ensure compliance and statistical success. Strong SAS or R programming skills are essential. #J-18808-Ljbffr...SASRemote work
- ...qualifying servers, storage systems, and high-performance networking platformsEngineering experience with: x86 server architecturesStorage - SAS, SATA, NVMe Networking - Ethernet, InfiniBand, RDMA, TCP, UDP Multicore - NUMA, memory management, caching PCIe Gen5/6Hypervisor...SASRemote work
- ...Python) to modernize clinical data programming technology. This remote, US-based role develops scalable Python solutions, transforms SAS workflows, and builds reusable data frameworks for SDTM-aligned deliverables. You will collaborate with global teams, establish coding...SASRemote work
- ...possible) to support clinical development programs. You will independently develop, program, and execute analyses and simulations using SAS, with opportunities to use R for additional work. Key tasks include Monte Carlo simulations, power calculations, MI techniques,...SASContract workRemote work
- ...coordinating research development with lead investigators, designing analytical approaches, and producing papers and presentations. You will develop SAS code, mentor junior analysts, and present findings to diverse audiences, including clinicians and sponsors. #J-18808-Ljbffr...SASRemote work
- ...of statistics, programming, and/or the clinical drug development process.Working knowledge of computing applications, including Base SAS, SAS/STAT, and SAS Macro Language.Strong organizational, interpersonal, leadership, and communication skills.Ability to manage multiple...SASRemote workWork from home
- ...multiple studies and collaborate with cross-functional teams to ensure timely, high-quality deliverables. Required MS/PhD in statistics/biostatistics with 4+ years in clinical statistics, strong regulatory knowledge, CDISC SDTM/ADaM, and SAS; R a plus. #J-18808-LjbffrSASRemote work
- ...years of experience in clinical trials. Responsibilities include overseeing study design and contributing to regulatory submissions. The position is for 6+ months, ideal for candidates with strong analytical skills and expertise in SAS and R programming. #J-18808-Ljbffr...SASRemote work
- Talantir is seeking a Clinical Programmer (SDTM) to provide comprehensive SAS-based programming support for global clinical trials. The role emphasizes ADaM specification development, TLG creation, and e-submission readiness while adhering to regulatory standards. The candidate...SASRemote job
- ...Responsibilities include statistical programming, validating programs, and collaborating across departments. Ideal candidates have proficient SAS programming skills and familiarity with clinical trial design. Benefits include a Health Care Plan, 401k Retirement Plan, and...SASRemote job
- ...datasets, ensuring data traceability and quality Perform statistical analysis and generate Tables, Listings, and Figures (TLFs) using SAS for Clinical Study Reports and regulatory submissions Required qualifications Bachelor's or Master's degree in Statistics,...SASFull timeRemote work
$114.4k - $124.8k
...Mandatory skills- SDTM, Clinical SAS, Python Job Description- Looking for SDTM experts having in-depth knowledge of sas programming(macro’s)1.Must have 6-8 yrs of exp in clinical domain 2.Strong knowledge of SDTM 3.Create advanced SAS macros, templates, and utilities for...SASFull timeRemote work- ...Python) to modernize clinical data programming technology. This remote US-based role focuses on scalable Python solutions, transforming SAS workflows, and building reusable frameworks for trial data delivery. You will contribute to CDISC SDTM-aligned datasets, coding...SASRemote work
- ...programs that maintain and use metadata repositories, including CRAN, pharmaverse, CDISC, MedDRA, and WHODrug metadataTranslate existing SAS macros and programs into validated, well-documented R functions and packages while maintaining the accuracy and reproducibility of...SASRemote workWorldwide
- ...: Smithfield Rhode IslandMUST HAVE: python developer, Informatica, SQL, Snowflake, python They will be evaluating a given product, a SAS product or it can be an AWS product, and they are evaluating to see if the product is good enough to have the FI organization use it....SASWork at officeWork from home
- ...is a hands‑on leadership role coordinating internal teams and biometrics vendors. The ideal candidate holds a PhD with 10–12 years in biostatistics within pharma/biotech/CRO, expert SAS/R skills, and a track record of successful regulatory submissions. #J-18808-Ljbffr...SASRemote work



