Associate RTSM Specialist – UK/US

Worldwide Clinical Trials

. Manage RTSM study amendments, ensuring deliverables are completed on time, within scope, and according to quality standards .

Posted 10/26/2026full-timeRemote • United Kingdom, United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in RTSM study management, including randomisation methodologies and clinical trial conduct, while ensuring compliance with quality standards and regulatory requirements. Strong communication and stakeholder management skills are essential for coordinating project activities and facilitating user acceptance testing.

Highest-signal resume keywords

RTSM ExperienceClinical Trial ConductStakeholder ManagementUser Acceptance Testing (UAT)Attention to Detail

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

RTSM Study DesignRandomisation MethodologiesBudget ManagementQuality Control ChecksData Integrity Principles

Soft Skills

Client-Facing SkillsCommunication SkillsAbility to Manage Multiple Priorities

Industry Keywords

Contract Research Organisation (CRO)Pharmaceutical EnvironmentPatient Safety RequirementsJust-In-Time Drug Supply Processes

About the role

Key responsibilities & impact

Manage RTSM study amendments, ensuring deliverables are completed on time, within scope, and according to 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 and drive issue resolution through completion
Monitor study randomisation processes to ensure accurate execution and study integrity
Create and execute User Acceptance Testing (UAT) plans and facilitate sponsor participation
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

Requirements

What you’ll need

Degree in a relevant discipline or equivalent combination of education and professional experience
Minimum 1 year of RTSM experience
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 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 ability to manage multiple priorities in a fast-paced environment

Benefits

Comp & perks

Collaborative and inclusive work environment
Growth and learning opportunities
Opportunity to take ownership of live RTSM projects
Opportunity to collaborate across functions and with global teams
Meaningful work contributing to life-changing clinical research