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Programmer • jacksonville fl

Last updated: 3 days ago

Clinical SAS Programmer

Katalyst HealthCares & Life SciencesJacksonville, FL
Full-time

Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s).Produces and delivers CDISC and regulatory compliant SDTM, and ADaM s...Show more

Statistical Programmer

Katalyst HealthCares & Life SciencesJacksonville, FL
Full-time

Our client, a leading Life Sciences Company, needs to hire a Statistical Programmer to provide programming support for Phase to Phase studies, including project integration and disease monitoring p...Show more

Senior Building Controls Technician (25% Travel)

The Building PeopleJacksonville, FL, US
Full-time

Senior Building Controls Technician .The position will work independently to meet project requirements with limited supervision.The programmer will be responsible for programming, configuring, and ...Show more

Application Programmer

Genesis10Jacksonville, FL
Permanent +1

Genesis10 is currently seeking an Automation Developer for a contract position with a Global Financial Institution located in Plano, TX, Jersey City, NJ and Jacksonville, FL.This is a 12+ month con...Show more

Audio Visual Programmer - Jacksonville

AnuVision Technologies Inc.Jacksonville, FL, US
Full-time
Quick Apply

We are seeking an experienced Audio Visual Programmer to join our team.The ideal candidate will design, develop, and implement custom programming solutions for Crestron, Extron, QSC, Biamp, and oth...Show more

Software Engineer/Applications Programmer 1

MaximusJacksonville, US
Full-time

Maximus TCS (Technology and Consulting Services) Internal Job Profile Code: TCS199, T1, Band 4 Job-Specific Essential Duties and Responsibilities: - Build and maintain simple UI components using Ja...Show more

Applications Development Lead (AI & Microservices) Assistant Vice President

00002 Citibank, N.A.Jacksonville Florida United States
Full-time

Citi, the leading global bank, has approximately 200 million customer accounts and does business in more than 160 countries and jurisdictions.Citi provides consumers, corporations, governments, and...Show more

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Clinical SAS Programmer

Clinical SAS Programmer

Katalyst HealthCares & Life SciencesJacksonville, FL
30+ days ago
Job type
  • Full-time
Job description

Responsibilities:
  • Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s)
  • Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets
  • Creates and validates tables, figures and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements
  • Provides input in the design and development of case report forms and clinical databases
  • Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs
  • Programs quality checks for clinical study raw data and report the findings to Data Management
  • Provides input in the design and development of case report forms and clinical study databases
  • Reviews or author eCRF, SDTM and ADaM datasets specifications for datasets programming
  • Provides programming support for adhoc analysis
  • Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group (, macros or graphical user interface applications)
  • Manages timelines and schedules of specific phases of projects with internal personnel and external vendors
  • Acts as lead programmer for a study
  • Reviews or validates statistical deliverables of vendors for assigned project(s)
Requirements:
  • MS in Statistics, Computer Science, or a related field with at least years or BS in Statistics, Computer Science, or a related field with at least years.
  • Experience in providing statistical programming support to early and late phase clinical trials.
  • Excellent skills in SAS programming and statistical reporting.
  • Knowledge of CDISC standards for SDTM and ADaM and FDA electronic data submission requirements.
  • Familiarity with FDA and ICH regulations and guidelines.
  • Excellent problem-solving skills.
  • Good written and verbal communication skills and organizational and documentation skills.
  • Ability to work on a multidisciplinary team that may include Biostatistics, Medical Directors, Data Management, Medical Writing, Pharmacovigilance, Clinical Operations, Medical Affairs, etc.
  • Ability to prioritize and multi-task effectively
  • Demonstrated positive attitude and the ability to work well with others.