Remote RTSM Specialist — Study Logistics & UAT

Worldwide Clinical Trials

Oregon

Hybrid

USD 60,000 - 90,000

Full time

13 days ago

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Job summary

Worldwide Clinical Trials is hiring an Associate RTSM Specialist to support RTSM solutions in global clinical trials. You will coordinate system updates, manage timelines, and collaborate with sponsors, study teams and partners to ensure regulatory compliance and data integrity.

This REMOTE role welcomes applicants from the UK or US. You will build a proactive approach to RTSM design, testing, and issue resolution, helping deliver patient-focused trials and maintain operational excellence across

Qualifications

  • Degree in a relevant discipline or equivalent experience.
  • Minimum 1 year RTSM experience in CRO/pharma environment.
  • Experience in CRO/pharma setting.
  • Knowledge of RTSM design, randomisation, just-in-time drug supply.
  • Understanding of trial conduct, blinding, patient safety, data integrity, regs.
  • Strong client-facing, communication, stakeholder skills.
  • Proficiency in English with strong written and verbal communication.

Responsibilities

  • Manage RTSM study amendments to time, scope, and quality.
  • Coordinate RTSM activities with sponsors, study teams, internal stakeholders.
  • Act as primary escalation point for RTSM maintenance.
  • Monitor study randomisation processes for accurate execution.
  • Create and execute UAT plans; involve sponsors in testing.
  • Review and approve study materials, helpdesk docs, system deliverables.
  • Perform financial reviews and support budget management for change orders.
  • Conduct quality checks and support study schedules and inventory.

Skills

RTSM experience
Communication skills
Stakeholder management
Attention to detail
Multitasking
English proficiency

Education

Degree in a relevant discipline

Job description

Worldwide Clinical Trials is hiring an Associate RTSM Specialist to support RTSM solutions in global clinical trials. You will coordinate system updates, manage timelines, and collaborate with sponsors, study teams and partners to ensure regulatory compliance and data integrity.

This REMOTE role welcomes applicants from the UK or US. You will build a proactive approach to RTSM design, testing, and issue resolution, helping deliver patient-focused trials and maintain operational excellence across

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