Java programming Jobs in Gainesville fl

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Java programming • gainesville fl

Last updated: 2 days ago

Promoted

Senior Manager, Clinical Programming

VirtualVocationsGainesville, Florida, United States

Full-time

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...Show moreLast updated: 2 days ago

Android Java Kotlin Mobile Developer

SherlockTalentHybrid South Florida

Full-time

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...Show moreLast updated: 30+ days ago

Promoted

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

InsideHigherEdGainesville, Florida, United States

Part-time

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...Show moreLast updated: 28 days ago

Java Developer - WMS Experienced Only

JASCIFL, US

Remote

Full-time

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...Show moreLast updated: 30+ days ago

Senior Manager, Clinical Programming

VirtualVocationsGainesville, Florida, United States

2 days ago

Job type

Full-time

Job description

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