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Java programming Jobs in Cape Coral, FL

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Java programming • cape coral fl

Last updated: 2 days ago
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Senior Manager, Clinical Programming

Senior Manager, Clinical Programming

VirtualVocationsFort Myers, 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
Developer Sr, JAVA Software

Developer Sr, JAVA Software

LCECNorth Fort Myers, FL, US
Full-time
JOB TITLE : Developer Sr, JAVA Software.M-F, Extra Hours as Needed and On-Call After-Hours Support Required.Company-wide annual incentive plan. Medical, vision and dental insurance.On-site wellness / m...Show moreLast updated: 30+ days ago
Android Java Kotlin Mobile Developer

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
Java Developer - WMS Experienced Only

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
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Senior Manager, Clinical Programming

Senior Manager, Clinical Programming

VirtualVocationsFort Myers, 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