Statistical Programming Jobs in USA

The Senior Research Analyst will support new pilots and scaled innovations with analyses that leverage rich data sources including national Medicare claims other payer claims electronic health records and event notification data.They will work cross-functionally with partners across o 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: Team provides customized real-world data and real-world evidence solutions to address the most important research questions across clinical development market access and commercial use cases for our life sciences partners. Independently translate analytic specificat More...

At Wyetech youll be at the center of an award-winning corporate culture breaking technological barriers and solving real-world problems for our federal government customers. We are committed to hiring the best of the best and in return we offer a world-class truly unique employee expe More...

PurposeThe Manager Statistics provides statistical expertise to support the research and development organization. Specific areas of work may include clinical trials patient safety and global medical affairs. The Manager works independently in partnership with experts in multiple disc More...

PurposeThe Manager Statistics provides statistical expertise to support the research and development organization. Specific areas of work may include clinical trials patient safety and global medical affairs. The Manager works independently in partnership with experts in multiple disc More...

The Director of Medical Affairs & Health Technology Assessment (MA&HTA) Statistics will be responsible for supporting AbbVies Medical Affairs activities in the Western European (EU WEC) and Intercontinental (INTERCON) regions. Additionally this role will assist with the EU HTA More...

The Director of Medical Affairs & Health Technology Assessment (MA&HTA) Statistics will be responsible for supporting AbbVies Medical Affairs activities in the Western European (EU WEC) and Intercontinental (INTERCON) regions. Additionally this role will assist with the EU HTA 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...

The Manager of Statistical Programming is a strategic role which guides a team of Statistical Programmers in the research and development of new pharmaceutical products. This role is directly responsible for leading the statistical programming activities for a compound/indication or t More...

Site: The General Hospital CorporationMass General Brigham relies on a wide range of professionals including doctors nurses business people tech experts researchers and systems analysts to advance our mission. As a not-for-profit we support patient care research teaching and community More...

The Senior Statistical Analyst is a key role in the research and development of new pharmaceutical products. The primary responsibilities for this role include the analysis and reporting of clinical trial data and leading the statistical programming activities for clinical studies and More...

Analyst Weber Shandwick Chicago (Hybrid)Youre curious organized methodical and proactive. You like to use substantiated data to both identify and solve problems rather than trust your gut alone.As the core team of global communications powerhouse Weber Shandwick we are leveraging ble More...

Department:106750 Clinical DevelopmentLocation:San Diego USA- RemoteBe a part of a global team that is inspired to make a difference in the lives of people living with rare disease.At Travere Therapeutics we recognize that our exceptional employees are vital to our success. We are a d More...

Responsibilities: Lead programming efforts for various clinical studies from Phase 1 to Phase 3 across multiple therapeutic areas. Develop and review annotated Case Report Forms (CRFs) and SDTM datasets ensuring accurate data representation. Program SDTM ADaM and TLFs and write detai 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...

Key Responsibilities: Work closely with a cross functional team within biostatistics data management and analytics to transition applications written in SAS or VBASIC to R. Conduct code review and technical assessment of legacy programs and suitability for migration to R. Recode appl 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. Statistical Programmer supports the Biostatistics team in the generation and validation of analysis datasets and statistical outputs for clinical trials. This role is key to implementing programming standards and supporting the standardization of CDISC-compl 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...