Remote RTSM Specialist for Global Clinical Trials

NCBioImpact; Durham (NC); Remote; USD 70.000 - 90.000; Vollzeit

Zusammenfassung

Worldwide Clinical Trials is seeking an Associate RTSM Specialist to drive RTSM implementations across global clinical trials. You will coordinate system updates, resolve issues, manage timelines, and support stakeholders across the study lifecycle, emphasizing data integrity and patient safety.

This remote role is open to candidates in the UK or US, enabling collaboration with global teams across multiple time zones.

Qualifikationen

• Minimum 1 year of RTSM experience in CRO or pharma setting.
• At least 2 years of experience within a CRO or pharmaceutical environment.
• Knowledge of RTSM study design, randomisation, and just-in-time drug supply.
• Understanding of clinical trial conduct, data integrity, and patient safety.
• Strong client-facing, communication, and stakeholder management skills.
• Fluency in English with excellent written and verbal communication.

Aufgaben

• Manage RTSM study amendments and ensure on-time delivery within scope.
• Coordinate RTSM activities with sponsors, study teams, and internal stakeholders.
• Serve as primary escalation point for RTSM maintenance and issue resolution.
• Monitor randomisation processes to ensure accurate execution and study integrity.
• Create and execute UAT plans, involving sponsor participation.
• Review and approve study materials, helpdesk docs, and system deliverables.
• Support budget management and change orders related financial reviews.
• Conduct QC checks, manage study schedules and inventory files.

Kenntnisse

RTSM experience

CRO/pharma environment

Project coordination

Stakeholder management

English proficiency

Ausbildung

Bachelor's degree in a relevant discipline

Jobbeschreibung

Worldwide Clinical Trials is seeking an Associate RTSM Specialist to drive RTSM implementations across global clinical trials. You will coordinate system updates, resolve issues, manage timelines, and support stakeholders across the study lifecycle, emphasizing data integrity and patient safety.

This remote role is open to candidates in the UK or US, enabling collaboration with global teams across multiple time zones.