Clinical SAS Programmer Jobs in USA

Roles & Responsibilities: Bachelors/Masters in Statistics CS Life Sciences or related field. 8-12 years clinical programming exp. with leadership exposure. Lead programming activities across studies and clinical development phases. Oversee CRO deliverables for quality timeliness and 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: Serve as the statistical programming lead on internal project teams and coordinate programming verification and documentation of statistical programs for use in creating analysis datasets tables listings and figures. Facilitate advanced technical expertise in conjun 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 Au More...

We are looking for a Senior SAS Programmer to join our Data Insights Team. Will work to support several reporting platforms. Programmer will create Excel and PDF reports using Base SAS as described by business requirements documents and test system components as needed. Responsi More...

We are looking for a Senior SAS Programmer to join our Data Insights Team. Will work to support several reporting platforms. Programmer will create Excel and PDF reports using Base SAS as described by business requirements documents and test system components as needed.Responsibiliti More...

Responsibilities: Cleaning and transforming raw clinical trial data from various sources to ensure accuracy and consistency for PK/PD analysis. Writing SAS code to perform descriptive analysis of PK/PD data and statistical analysis of exposure-response relationships. Data visualizati 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: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 statistic 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 statistic More...

Responsibilities: Lead the development and implementation of submission-ready SDTM datasets in accordance with regulatory requirements (e.g. FDA EMA PMDA). Collaborate with regulatory affairs and quality assurance teams to ensure compliance with submission guidelines and standards. P 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. Contribu More...

Responsibilities: Creation of SAS programs to Develop or Validate SDTM/Adam/TLFs. Provide oversight for CRO SDTM/Adam/TLFs deliverables for multiple studies and make sure efficiencies are gained at project level. Generate and/or review of SDTM mapping specifications annotated CRFs Ad More...

Anticipated End Date:Position Title:Medical Coding Analyst SR. 100% Virtual CareBridgeJob Description:CareBridge Health is a proud member of the Elevance Health family of companies within our Carelon business. CareBridge Health exists to enable individuals in home and community-based More...

Work with one of our preferred clients! Our client is a leading pharmaceutical/biotech company dedicated to advancing medical science and improving patient outcomes through the development of innovative therapeutics. Their research-driven organization focuses on discovering developing More...

Responsibilities: Support the Lead Data Manager across one or more clinical studies. Reviews protocols for appropriate data capture including electronic (eCRF) design. Support CRF design review and validation of clinical database. Provide expertise and support oversight of database s More...

Are you driven to make a meaningful impact in the lives of individuals with mental health and intellectual/developmental disabilities (IDD) Easterseals PORT Health is hiring Direct Support Professionals (DSPs) to join our compassionate team in Wilmington.We are hiring for the followin More...

Serious Medicine is what we do. Being extraordinary is who we are. Every colleague plays a key role in upholding this promise to our patients and their families.Shift:First Shift (United States of America)ShiftDetails:M-F 8am - 5pmHybrid after training.Why Work at Nebraska MedicineTog More...

Current Employees:If you are a current Staff Faculty or Temporary employee at the University of Miami please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position using the Career worklet please review this tip s More...