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Java programming Jobs in Clearwater, FL
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Java programming • clearwater fl
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Senior Manager, Clinical Programming
VirtualVocationsClearwater, Florida, United StatesIndustry X Software Developer MES Aveva Programming Specialist / Associate Manager
AccentureSt. Pete, 140 Fountain Pkwy, Tampa CorpAndroid Java Kotlin Mobile Developer
SherlockTalentHybrid South FloridaProgramming Job Training Program
Year Up UnitedSafety Harbor, FL, USSenior Java Developer
Two95 International Inc.Largo, Florida, United StatesJava Developer - WMS Experienced Only
JASCIFL, USJava Architect -Remote Role - Contract
Isofttek Solutions IncLargo, Florida, United StatesJava / Angular Full Stack Developer - US Citizenship Required
Ignite ItLargo, Florida, United States- general dentist (from $ 47,500 to $ 264,500 year)
- social media (from $ 43,425 to $ 250,000 year)
- business development director (from $ 62,500 to $ 228,500 year)
- project scheduler (from $ 89,213 to $ 180,000 year)
- hospital (from $ 33,657 to $ 175,500 year)
- seasonal (from $ 29,250 to $ 175,500 year)
- dentist (from $ 111,150 to $ 175,000 year)
- physician assistant (from $ 100,000 to $ 171,278 year)
The average salary range is between $ 90,000 and $ 162,565 year , with the average salary hovering around $ 120,938 year .
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Senior Manager, Clinical Programming
VirtualVocationsClearwater, 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
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