Remote RTSM Specialist - Associate

Worldwide Clinical Trials; United States; Remote; USD 65.000 - 90.000; Vollzeit

Zusammenfassung

Worldwide Clinical Trials is seeking an Associate RTSM Specialist to deliver RTSM solutions for global clinical trials. You will coordinate system updates, manage timelines, and support stakeholders across the study lifecycle.

You will work with sponsors and internal teams to ensure data integrity, patient safety, and regulatory compliance while maintaining project timelines and quality standards.

Qualifikationen

• Degree in a relevant discipline or equivalent combination of education and professional experience.
• Minimum 1 year of RTSM experience and at least 2 years of experience within a CRO or pharmaceutical environment.
• Experience working within a Contract Research Organisation (CRO) or pharmaceutical setting.
• Knowledge of RTSM study design, randomisation methodologies, and just-in-time drug supply processes.
• Understanding of clinical trial conduct, blinding practices, patient safety requirements, data integrity principles, and applicable regulations.
• Demonstrated ability to manage and support the delivery of RTSM solutions used in clinical trials.
• Strong client-facing, communication, and stakeholder management skills.
• Proficiency in English, with strong written and verbal communication skills, excellent attention to detail, and the ability to manage multiple priorities in a fast-paced environment.

Aufgaben

• Manage RTSM study amendments, ensuring deliverables are completed on time, within scope, and in accordance with established quality standards.
• Coordinate and communicate RTSM project activities with sponsors, study teams, and internal stakeholders.
• Serve as the primary escalation point for RTSM maintenance activities, driving issue resolution through to completion.
• Monitor study randomisation processes to ensure accurate execution and support study integrity.
• Create and execute User Acceptance Testing (UAT) plans and facilitate sponsor participation in testing activities.
• Review, prepare, and approve study support materials, helpdesk documentation, and system-related deliverables.
• Perform financial reviews and support budget management activities related to change orders.
• Conduct quality control checks, process study schedules and inventory files, and support ongoing operational activities as required.

Kenntnisse

RTSM experience

Client-facing

Communication

Stakeholder management

Ausbildung

Bachelor degree or equivalent

Jobbeschreibung

Worldwide Clinical Trials is seeking an Associate RTSM Specialist to deliver RTSM solutions for global clinical trials. You will coordinate system updates, manage timelines, and support stakeholders across the study lifecycle.

You will work with sponsors and internal teams to ensure data integrity, patient safety, and regulatory compliance while maintaining project timelines and quality standards.