Remote RTSM Specialist — Clinical Trial Support

Worldwide Clinical Trials; Durham (NC); Remote; USD 70,000 - 95,000; Full time

Job summary

Worldwide Clinical Trials is seeking an Associate RTSM Specialist to support RTSM solutions across global trials. You will coordinate system updates, resolve issues, manage timelines, and support stakeholders throughout the study lifecycle to ensure regulatory compliance, data integrity, and patient safety.

You will work with internal teams, sponsors, and external partners to deliver high-quality RTSM services, taking ownership of live projects and contributing to operational excellence in

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 in a CRO or pharmaceutical environment.
• Experience in CRO or pharmaceutical setting and knowledge of RTSM design and randomisation.
• Understanding of clinical trial conduct, blinding, patient safety, data integrity and regulations.

Responsibilities

• Manage RTSM study amendments, ensuring deliverables are on time and within quality standards.
• Coordinate RTSM project activities with sponsors, study teams, and internal stakeholders.
• Serve as primary escalation point for RTSM maintenance activities and issue resolution.
• Monitor study randomisation processes to ensure accurate execution and study integrity.
• Create and execute User Acceptance Testing (UAT) plans and involve sponsor in testing.
• Review and approve study support materials, helpdesk documentation and system deliverables.
• Conduct financial reviews and support budget management related to change orders.
• Perform quality control checks and support ongoing operational activities.

Skills

RTSM experience

Stakeholder management

Client communication

Attention to detail

Multi-priority handling

Education

Relevant degree in life sciences

Job description

Worldwide Clinical Trials is seeking an Associate RTSM Specialist to support RTSM solutions across global trials. You will coordinate system updates, resolve issues, manage timelines, and support stakeholders throughout the study lifecycle to ensure regulatory compliance, data integrity, and patient safety.

You will work with internal teams, sponsors, and external partners to deliver high-quality RTSM services, taking ownership of live projects and contributing to operational excellence in