Remote Clinical IRT & Supply Systems Specialist

IQVIA Inc; Reading; Hybrid; GBP 55,000 - 75,000; Full time

Job summary

IQVIA is seeking a Clinical Supply IRT Specialist to support clinical trials through Interactive Response Technology (IRT) and clinical supply management.

You will partner with cross-functional study teams to support IRT setup, change management activities, system validation, and process optimization. You will act as a subject matter expert, helping ensure that clinical supply strategies are translated into system requirements while maintaining quality, compliance, and operational efficiency.

Qualifications

• Experience within clinical research, clinical supplies, clinical operations, or a related pharmaceutical/biotechnology environment.
• Knowledge of clinical trial processes and the drug development lifecycle.
• Familiarity with Interactive Response Technology (IRT), RTSM, IVRS/IWRS, or similar clinical trial systems.
• Strong analytical and problem-solving skills with the ability to manage multiple priorities.
• Experience collaborating with cross-functional and global stakeholders.
• Excellent communication and stakeholder management abilities.
• Strong attention to detail and a quality-focused mindset.
• Proficiency with clinical systems and standard business applications.

Responsibilities

• Support the design, setup, and maintenance of IRT solutions for clinical studies.
• Collaborate with study teams and stakeholders to translate operational and supply requirements into IRT specifications.
• Contribute to risk assessments and support user acceptance testing (UAT) activities for new study setups and system changes.
• Review, develop, and execute testing documentation and associated validation activities as required.
• Provide guidance and expertise on IRT-related processes, systems, and best practices.
• Partner with internal and external stakeholders to support study startup, amendment implementation, and ongoing study management.
• Contribute to continuous improvement initiatives aimed at enhancing IRT processes, tools, and ways of working.
• Support training activities and knowledge sharing across study teams and functional groups.
• Ensure activities are conducted in compliance with applicable quality standards, Good Clinical Practice (GCP), and regulatory requirements.

Skills

Clinical research

IRT systems

Stakeholder management

Analytical skills

Cross-functional collaboration

Attention to detail

Clinical systems

Job description

IQVIA is seeking a Clinical Supply IRT Specialist to support clinical trials through Interactive Response Technology (IRT) and clinical supply management.

You will partner with cross-functional study teams to support IRT setup, change management activities, system validation, and process optimization. You will act as a subject matter expert, helping ensure that clinical supply strategies are translated into system requirements while maintaining quality, compliance, and operational efficiency.