Remote RTSM Associate — Global Clinical Trials

Worldwide Clinical Trials Limited; United Kingdom; À distance; GBP 42 000 - 66 000; Plein temps

Résumé du poste

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

The role covers live RTSM projects, UAT planning, change orders, and budget-related activities, with remote work from UK or US.

Qualifications

• 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.

Responsabilités

• 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.

Connaissances

Client-facing

Communication skills

Stakeholder mgmt

Formation

Bachelor's degree

Description du poste

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

The role covers live RTSM projects, UAT planning, change orders, and budget-related activities, with remote work from UK or US.