Cnc programmer Empleos en Pearland tx

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Cnc programmer • pearland tx

Última actualización: hace 1 día

Principal Statistician Programmer

VirtualVocationsPasadena, Texas, United States

A tiempo completo

A company is looking for a Principal Statistician Programmer for 100% remote work.Key Responsibilities Provide statistical support in protocol development for observational studies and clinical t...Mostrar másÚltima actualización: hace 1 día

Senior Systems Programmer Analyst - CDS

BlueCross BlueShield of South CarolinaTexas

A tiempo completo

IT solutions and managed services.We operate multiple geographically disperse data centers, including two of the nation’s largest healthcare data centers – both rated among the top five percent of ...Mostrar másÚltima actualización: hace más de 30 días

SENIOR APPLICATION PROGRAMMER ANALYST (GIS)

Tarrant CountyTarrant County, TX

A tiempo completo

The Senior Application Programmer Analyst is responsible for the planning, architecture, development, maintenance and support of complex applications for the enterprise delivered via the web, Inter...Mostrar másÚltima actualización: hace más de 30 días

CNC Machinist / Operator

John CranePasadena, Texas, United States

A tiempo completo

Sets up, writes programs and edits existing programs, and operates numerically controlled machinery.These include but are not limited to lathes, mills, drills, and other machinery as required.Maint...Mostrar másÚltima actualización: hace más de 30 días

CNC Machinist Second Shift

FlowservePasadena, Texas US

A tiempo completo

Set up and operate a variety of machine tools to produce precision parts and instruments.Includes precision instrument makers who fabricate, modify, or repair mechanical instruments.May also fabric...Mostrar másÚltima actualización: hace más de 30 días

Principal Statistician Programmer

VirtualVocationsPasadena, Texas, United States

Hace 1 día

Tipo de contrato

A tiempo completo

Descripción del trabajo

A company is looking for a Principal Statistician Programmer for 100% remote work.

Key Responsibilities

Provide statistical support in protocol development for observational studies and clinical trials

Author and review statistical analysis plans, analysis dataset specifications, and TFL shells

Conduct programming and analysis for Medical Affairs and Real World Evidence studies

Required Qualifications

PhD or MS in Biostatistics or Statistics

Minimum 4 years of experience in the pharmaceutical industry with interventional and observational studies

Minimum 4 years of experience with Phase-4 studies, Medical Affairs studies, or Real World Evidence methodologies

Minimum 4 years of experience with statistical software, specifically SAS and R

Minimum 4 years of experience with advanced statistical models and Real World Data methodologies