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Programmer • rochester ny

Last updated: 2 days ago

Statistical Programmer

Katalyst HealthCares & Life SciencesRochester, NY
Temporary

The Statistical Programmer will contribute expert programming skills to deliver accurate, regulatory-compliant clinical data outputs for Compass Pathways development programs.The role requires stro...Show more

Programmer Analyst

TradeJobsWorkForce14605 Rochester, NY, US
Full-time

Programmer Analyst Job Duties: Identifies requirements by establishing personal rapport with potential and actual clients and with other persons in a position to understand service requirements.Arr...Show more

 • Promoted

Software Engineer/Applications Programmer 1

MaximusRochester, 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

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Statistical Programmer

Statistical Programmer

Katalyst HealthCares & Life SciencesRochester, NY
30+ days ago
Job type
  • Temporary
Job description

Job Description:
The Statistical Programmer will contribute expert programming skills to deliver accurate, regulatory-compliant clinical data outputs for Compass Pathways development programs. The role requires strong technical proficiency, collaboration across teams, and adaptability to support complex clinical trial requirements.
Responsibilities:
  • Leading and coordinating the programming activities within agreed timelines.
  • Managing the reporting of studies internally and externally.
  • Programming outputs as stated in the analysis plan.
  • Working closely with study team members, mainly with the study statistician.
  • Reviewing of the Statistical Analysis Plan (SAP) and shells.
  • Create and review SDTM and ADaM study specifications.
  • Ensure programs, datasets, outputs are appropriate for regulatory submission.
  • Perform simulations and data modelling.
  • Perform Interim analyses.
  • Liaise with external vendors on deliverables.
Requirements:
  • Bachelor's/master's degree in a Scientific Discipline.
  • + years' experience in statistical programming.
  • CDISC expertise.
  • Proficient in programming including performing statistical analyses and creating macros in SAS, preferably R.
  • Programming/reporting expertise across all phases of clinical development (efficacy/safety/PK), including ISS/Client reporting.
  • Experience in performing quality control (QC) checks.
  • Extensive knowledge in regulatory submission process.
  • Good understanding of ICH guidelines and regulations such as CFR Part .
  • Experience supporting NDA submissions , FDA, EMA, MHRA and addressing regulatory questions.
  • Ability to solve challenging problems and provide recommendations to mitigate risk.
  • Good communication skills - both written and verbal.
  • Team works skills - Including cross-functional and within the Statistics and Data Management Team.