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Java programmer • london on

Last updated: 2 hours ago

SDTM Programmer

Connect Life SciencesLondon, CA
Full-time

Overview: We are seeking an experienced SDTM Programmer to support clinical trial data standardization and regulatory submissions.This individual will be responsible for transforming raw clinical ... Show more

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Controls and Robotics Programmer (Automation Systems Programmer)

BOS InnovationsLondon, ON, CA
CA$40.00 hourly
Full-time
Quick Apply

We’re looking for a Senior PLC & Robotics programmer who owns automation projects end-to-end, from concept and programming to commissioning and customer handoff.At BOS Innovations, we design an... Show more

Manufacturing Technician / Technologist, CNC Programmer, Machinist

Kawartha ControlsLondon, CA
Full-time

G-code validation, CNC Machine Setup/operation.Hydraulics / Fluid Power application design, Schematics, · Fixtures, Robotics, Automation, Mechatronics and Hydraulic component & system estimating, ... Show more

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ERP and Application Developer

Sailun Tire AmericasLondon, CA
Full-time

Sailun Tire Americas – ERP and Application Developer Position Reporting To – Director of IT Summary/Objective We are looking for an experienced Java Developer with strong ERP systems knowledge t... Show more

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Software Engineer II (Mainframe)

The Toronto-Dominion Bank (Canada)London, Ontario
Full-time

TD’s Core Platform Party1 Product Group is seeking a talented Software Engineer II to support mission-critical applications including CIF (CustomerLink) , PRTCL (Party API ) and others.This role of... Show more

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SDTM Programmer

SDTM Programmer

Connect Life SciencesLondon, CA
2 hours ago
Job type
  • Full-time
Job description
Overview: We are seeking an experienced SDTM Programmer to support clinical trial data standardization and regulatory submissions. This individual will be responsible for transforming raw clinical data into CDISC-compliant SDTM datasets and ensuring high-quality, submission-ready deliverables. The role requires strong collaboration with Data Management, Biostatistics, and Clinical teams. Key Responsibilities: • Develop, validate, and maintain SDTM datasets in compliance with CDISC standards • Convert raw clinical trial data into SDTM format using SAS programming • Create and maintain SDTM specifications (mapping specifications, define.xml, SDRG) • Perform quality control (QC) and validation of SDTM datasets and outputs • Ensure datasets meet regulatory submission requirements (FDA, EMA) • Collaborate with Data Management to review CRFs and ensure proper data collection for SDTM mapping • Work closely with Biostatistics and ADaM programmers to support downstream analyses • Troubleshoot data issues and ensure data integrity, consistency, and traceability • Support submission activities, including reviewer’s guides and regulatory documentation • Contribute to process improvements and standardization initiatives Required Qualifications: • Bachelor’s degree in Statistics, Computer Science, Life Sciences, or related field • 6-7+ years of SAS programming experience within the pharmaceutical or biotech industry • Hands-on experience with CDISC SDTM standards and implementation • Strong knowledge of clinical trial data structures and data flow • Experience creating define.xml and SDTM documentation (SDRG) • Familiarity with regulatory submission requirements (FDA, EMA) • Experience working in a CRO or sponsor environment • Strong attention to detail and problem-solving skills and lead experience • Excellent communication and ability to work cross-functionally Preferred Qualifications: • Experience with ADaM datasets and TLF generation • Oncology or other therapeutic area experience • Experience with Pinnacle 21 (validation tool) • Knowledge of additional programming languages (e.g., R) is a plus • Prior experience supporting NDA/BLA submissions