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Java programming • gainesville fl

Última actualización: hace 2 días
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Senior Manager, Clinical Programming

Senior Manager, Clinical Programming

VirtualVocationsGainesville, Florida, United States
A tiempo completo
A company is looking for a Senior Manager, Clinical Programming.Key Responsibilities Develop and implement Study Data Tabulation Model (SDTM) standards ensuring compliance with industry standards...Mostrar másÚltima actualización: hace 2 días
Android Java Kotlin Mobile Developer

Android Java Kotlin Mobile Developer

SherlockTalentHybrid South Florida
A tiempo completo
Mobile Developer Android JAVA & Kotlin.Do you love developing valuable solutions to make it easy for mobile users to control their world from anywhere?. Do you live / want to live / in South Florida an...Mostrar másÚltima actualización: hace más de 30 días
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WRUF AM and FM : OPS / Part-Time Programming Assistant

WRUF AM and FM : OPS / Part-Time Programming Assistant

InsideHigherEdGainesville, Florida, United States
A tiempo parcial
WRUF AM and FM : OPS / Part-Time Programming Assistant.Communications / Public Relations / Marketing, Office / Administrative / Fiscal Support. WRUF AM and FM : OPS / Part-Time Programming Assistant.Classificatio...Mostrar másÚltima actualización: hace 28 días
Java Developer - WMS Experienced Only

Java Developer - WMS Experienced Only

JASCIFL, US
Teletrabajo
A tiempo completo
Quick Apply
JASCI is a leading provider of Warehouse Management software solutions for the logistics market, serving some of the largest companies in the world. We are currently seeking a qualified Java Develop...Mostrar másÚltima actualización: hace más de 30 días
Senior Manager, Clinical Programming

Senior Manager, Clinical Programming

VirtualVocationsGainesville, Florida, United States
Hace 2 días
Tipo de contrato
  • A tiempo completo
Descripción del trabajo

A company is looking for a Senior Manager, Clinical Programming.

Key Responsibilities

Develop and implement Study Data Tabulation Model (SDTM) standards ensuring compliance with industry standards

Ensure alignment of SDTM standards with data collection standards and provide SDTM mapping guidance

Serve as a subject matter expert on standards development and facilitate continuous process improvement

Required Qualifications

Bachelor's degree in Statistics, Computer Science, or Life Sciences; Master's degree preferred

At least 6-8 years of relevant experience in the pharmaceutical, biotech, CRO, or Regulatory Agency

Proficient in SAS programming with 6-8 years of experience

Practical knowledge of R to support clinical trials preferred

Demonstrated knowledge of clinical research, metadata management, and regulatory requirements