At a Glance
- Tasks: Support clinical trials by managing Interactive Response Technology and optimising supply processes.
- Company: Join IQVIA, a leader in transforming healthcare through data and technology.
- Benefits: Collaborative environment, career growth, and the chance to impact patient outcomes.
- Other info: Opportunity to work with industry experts and contribute to innovative medical treatments.
- Why this job: Make a difference in clinical research while developing your expertise in a global setting.
- Qualifications: Experience in clinical research or related fields; strong analytical and communication skills.
The predicted salary is between 49941 - 61039 £ per year.
IQVIA is seeking a Clinical Supply IRT Specialist to support the successful delivery of clinical trials through expertise in Interactive Response Technology (IRT) and clinical supply management processes. In this role, 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 accurately translated into system requirements while maintaining quality, compliance, and operational efficiency. This position offers an excellent opportunity for professionals with experience in clinical supplies, clinical operations, or IRT systems who enjoy working at the intersection of technology and clinical trial delivery.
Key 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.
Qualifications & Experience Required
- 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.
Preferred
- Experience supporting clinical supply chain activities.
- Exposure to study startup and system validation activities.
- Understanding of GCP, GMP, and applicable regulatory requirements.
- Experience contributing to process improvement initiatives and training activities.
- Previous experience working within global clinical development organizations.
What You'll Bring
- A collaborative and proactive approach to problem-solving.
- The ability to navigate complex processes and technical systems.
- Strong organizational skills and attention to detail.
- A passion for improving clinical trial operations and supporting the delivery of medicines to patients.
Why Join IQVIA?
At IQVIA, you'll work alongside industry-leading experts who are transforming healthcare through data, technology, and clinical research. You'll have the opportunity to contribute to innovative clinical programs while growing your expertise in a highly collaborative and global environment. Join us and help accelerate the development of therapies that make a difference for patients worldwide.
Clinical Supply IRT Specialist in Reading employer: IQVIA
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that prioritises innovation and employee well-being. Our South West England location provides flexible working arrangements, comprehensive well-being support, and robust career development opportunities through our AI-powered talent marketplace, ensuring that you can thrive both personally and professionally while contributing to meaningful advancements in healthcare.
