Clinical SAS Programmer Jobs in USA

Required AttachmentsDocuments required for this position are listed under the Required Attachments section of this job listing. You will be required to upload and attach these documents in the application process.Important: ALL required documents must be attached to your job applicati More...

Responsibilities: Develop and maintain SAS programs to import clean and validate clinical trial data. Use R for data manipulation analysis and visualization. Perform statistical analyses in accordance with study protocols and analysis plans. Generate tables listings and figures (TLFs More...

Responsibilities: Providing statistical programming support to generate tables listings and figures for assigned projects. Demonstrating proficiency in CDISC SDTM and ADaM to support various submission activities including IA CSR DSUR and publications. Overseeing all aspects of stati More...

Responsibilities: Effectively designs and codes SAS programs using BASE/SAS SAS/STAT SAS/GRAPH and SAS MACROS for assigned clinical projects(s). Produces and delivers CDISC and regulatory compliant SDTM and ADaM standard datasets. Creates and validates tables figures and listings (TF More...

OverviewSenior Cybersecurity Analyst IT CybersecurityFull Time 80 Hours Per Pay Period Day ShiftCovenant Health Overview:Covenant Health is the regions top-performing healthcare network with 10hospitalsoutpatient and specialtyservicesandCovenant Medical Group our areas fastest-growing More...

DepartmentBusiness AnalyticsEmployment TypeFull TimeLocationDallasWorkplace typeHybridCompensation$70000 - $90000 / yearReporting ToMichael Horan Key Responsibilities Job Qualifications Benefits About Group O At Group O its ou More...

Responsibilities: Effectively designs and codes SAS programs using BASE/SAS SAS/STAT SAS/GRAPH and SAS MACROS for assigned clinical projects(s). Produces and delivers CDISC and regulatory compliant SDTM and ADaM standard datasets. Creates and validates tables figures and listings (TF More...

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. Contribut More...

Boys Town National Research Hospital is seeking an experienced Epic Clinical Systems Training and Support Specialist (Ambulatory). This is a crucial role for ensuring our staff is proficient in utilizing Epic systems while enhancing their productivity and workflow efficiency. The ide More...

Responsibilities: Effectively manage and oversee statistical programming resources including contractors and CROs related to statistical programming deliverables to ensure high-quality within timeline and budget. Conduct hands-on validation/QC of CRO deliverables to ensure high-quali More...

Responsibilities: The Principal SAS Programmer will be responsible for statistical programming for the clients clinical studies. In this role you will develop and validate SAS programs for data presentation analyses and provide programming support to project team members. Our Ideal c More...

Responsibilities: Effectively designs and codes SAS programs using BASE/SAS SAS/STAT SAS/GRAPH and SAS MACROS for assigned clinical projects(s). Produces and delivers CDISC and regulatory compliant SDTM and ADaM standard datasets. Creates and validates tables figures and listings (TF More...

Responsibilities:Effectively designs and codes SAS programs using BASE/SAS SAS/STAT SAS/GRAPH and SAS MACROS for assigned clinical projects(s).Produces and delivers CDISC and regulatory compliant SDTM and ADaM standard datasets.Creates and validates tables figures and listings (TFLs) More...

Responsibilities: Providing statistical programming support to generate tables listings and figures for assigned projects. Demonstrating proficiency in CDISC SDTM and ADaM to support various submission activities including IA CSR DSUR and publications. Overseeing all aspects of stati More...

Responsibilities: Position leads complex studies in study design statistical analysis and interpretation of results with some supervision. This position contributes to specific aspects of drug development plans with minimal supervision and contributes to documents submitted to Health More...

Responsibilities: 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 More...

Responsibilities: Review protocols for CDISC conformance. Review Case Report Forms and eCRFs with CDISC CDASH and SDTM conformant elements. Write and manage SAS code for mapping clinical data to SDTM data structures in conformance with Emmes SDTM Implementation Guide project standard More...

Responsibilities: The Sr. SAS Programmer will be responsible for statistical programming for the clients clinical studies. In this role you will develop and validate SAS programs for data presentation analyses and provide programming support to project team members. Our Ideal candida More...

Responsibilities:The Sr. SAS Programmer will be responsible for statistical programming for the clients clinical studies.In this role you will develop and validate SAS programs for data presentation analyses and provide programming support to project team members.Our Ideal candidate w More...

Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming support for publication efforts and regulatory submissions. Manage the timely creation review completion and delivery of statistical programming activities and deliverable More...