Senior Manager, Interactive Response Technology (IRT/RTSM)

Tucker Parker Smith Group (TPS Group)
  • San Rafael, CA
  • Remote
  • $76 Per Hour
  • Instant Apply
6 days ago

Job Description

Senior Manager, Interactive Response Technology (IRT/RTSM)

Location: 100% Remote
Contract: 12-month W2 assignment
Pay Rate: $76/hour DOE & location

About the Role

Seeking an experienced IRT/RTSM professional to manage the design, implementation, and lifecycle of Interactive Response Technology systems supporting Phase I IV clinical trials. This is a hands-on individual contributor role with responsibility for IRT activities from study setup through closeout.

Responsibilities

" Lead IRT/RTSM activities from study kickoff through closeout.
" Translate clinical protocols into User Requirement Specifications (URS).
" Manage IRT vendors, study builds, timelines, configurations, and deliverables.
" Develop test plans and lead User Acceptance Testing (UAT).
" Support randomization, blinding, dosing, enrollment, inventory, and drug resupply activities.
" Troubleshoot IRT issues during active clinical trials.
" Manage system changes resulting from protocol amendments.
" Partner with Clinical Supply Chain to optimize inventory and resupply strategies.
" Lead IRT closeout, reconciliation, archival, and decommissioning activities.
" Maintain IRT standards, SOPs, work instructions, test scripts, and training materials.
" Partner with Clinical Operations, Supply Chain, IT, Data Management, Biostatistics, Quality, and external vendors.

Required Qualifications

" Bachelor's degree in life sciences, engineering, supply chain, information systems, or related field.
" 5+ years of hands-on IRT/RTSM experience across multiple clinical studies.
" End-to-end IRT experience including URS, study builds, UAT, go-live, study support, change control, and closeout.
" Knowledge of randomization, blinding, clinical drug supply, forecasting, and IRT resupply strategies.
" Experience managing external IRT/RTSM vendors.
" Knowledge of GCP, 21 CFR Part 11, computer system validation, and clinical system compliance.
" Strong project management, communication, and cross-functional collaboration skills.

Preferred Qualifications

" Experience with multiple commercial IRT/RTSM platforms.
" Rare disease, gene therapy, or global clinical trial experience.
" Experience with IRT integrations to EDC, CTMS, ERP, or supply planning systems.
" Experience with decentralized trials, direct-to-patient supply, drug pooling, or adaptive trial designs.

Numbers & Facts

LocationSan Rafael, CA (
Remote
)

Skills

  • Acceptance Testingunmatched
  • Biologyunmatched
  • Biostatisticsunmatched
  • Change Controlunmatched
  • Change Managementunmatched
  • Clinical Information Systemsunmatched
  • Clinical Practices/Protocolsunmatched
  • Clinical Trialunmatched
  • Code of Federal Regulationsunmatched
  • Computer Systemsunmatched
  • Cross-Functionalunmatched
  • Data Managementunmatched
  • Diseaseunmatched
  • ERP (Enterprise Resource Planning)unmatched
  • Electronic Data Capture (EDC)unmatched
  • Forecastingunmatched
  • GCP (Good Clinical Practices)unmatched
  • Gene Therapyunmatched
  • Identify Issuesunmatched
  • Information Technology & Information Systemsunmatched
  • Phase I Clinical Trialsunmatched
  • Phase IV Clinical Trialsunmatched
  • Project/Program Managementunmatched
  • Reconciliationunmatched
  • Standard Operating Procedures (SOP)unmatched
  • Supply Chainunmatched
  • Supply Chain Operationsunmatched
  • Supply Chain Optimizationunmatched
  • System Validationunmatched
  • Systems Administration/Managementunmatched
  • Team Playerunmatched
  • Technical Supportunmatched
  • Test Plan/Scheduleunmatched
  • Test Scriptsunmatched
  • Testingunmatched
  • Vendor/Supplier Managementunmatched

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