AstraZeneca

Specialist,GlobalClinicalSolutions(IRT)

$105–145k ~AI est. Warsaw, Poland FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Entry candidates.

The Brief

“Specialist, Global Clinical Solutions (IRT) at AstraZeneca. Skills: IRT/RTSM, Study lifecycle management, Vendor management. Support study teams. Set-up IRT system”

What You'll Achieve.

Safeguard data integrity; Safeguard inspection readiness; Streamline operational processes; Streamline operational tools; Accelerate study delivery; Strengthen user capability; Strengthen user adoption

Industry & Context.

Problems you'll solve

Risk identification; Issue identification; Solution identification

What They're Looking For.

Must Have

Bachelor's degree or equivalent, Organizational and analytical skills, Multitasking and time management, Excellent spoken and written communication, Demonstrated alignment with AZ Values, Prior administrative training/experience

Nice to Have

Degree in biological sciences, Degree in healthcare-related field, Understanding of clinical study processes, Pharmaceutical knowledge of regulations, GxP training, Experience in pharma environments, Experience in clinical development environments, Ability to train others, Proactively identify risks/issues and solutions

What You'll Do.

Drive vendor management

Ensure performance quality compliance

Ensure timely delivery

Ensure consistent service delivery

Ensure complete service delivery

Ensure high-quality service delivery

Partner with study teams

Partner with external vendors

Maintain systems/tools

Validate systems/tools

Manage lifecycle of systems/tools

Manage business continuity

Manage standards of systems/tools

Manage procedural/system documentation

Deliver process/system/tool training

Facilitate knowledge sharing

Establish best practices

Support effective communication

Analyze usage for efficiency

Analyze usage for effectiveness

Contribute to user requirements

Support business cases for improvement

Contribute to change initiatives

How You'll Work.

Team & Collaboration

Partner with Study Teams; Partner with external vendors; Support study teams; Support user communities; Support Clinical Operations

Communication Scope

Spoken communication; Written communication

Process & Methodology

Planning, Risk tracking, Issue tracking, Stakeholder communication

Full Job Description

**Job Title:** Specialist, Global Clinical Solutions (IRT/RTSM) **Location** : Warsaw, Poland **H** ybrid model of work: 3 days in office, 2 remote per week ## **Introduction to role** Global Clinical Solutions (GCS) drives the delivery of centralized services and technology that enable Clinical Operations to execute development programs to time, cost, and quality. As a **Specialist** in GCS focused on **Interactive Response Technology (IRT)/Randomization & Trial Supply Management (RTSM)**, you will ensure high‑quality, complete operational data; robust lifecycle management of systems and processes; and effective training and adoption across user communities. We are recruiting IRT Leads to oversee study‑specific IRT/RTSM solutions that manage randomization, drug supply, and site/subject activities across clinical studies. You will **support study teams** through the full lifecycle—**set‑up, maintenance, and close‑out** —of the IRT system tailored to each protocol. You will drive **vendor management** to ensure performance, quality, compliance, and timely delivery across IRT providers. The role requires emerging**project management** capability—bring at least one demonstrable skill (for example, planning, risk/issue tracking, or stakeholder communication) and a strong willingness to learn and develop the others. **Impact** : You will safeguard data integrity and inspection readiness, streamline operational processes and tools to accelerate study delivery, and strengthen user capability and adoption across Clinical Operations. **What you’ll do** * Service delivery across drug projects: ensure consistent, complete, and high‑quality Clinical Operations data; partner with Study Teams and external vendors. * Systems and tools enablement: set up, maintain, validate, and test Clinical Operations systems/tools; manage lifecycle, business continuity, standards, and procedural/system documentation. * Training and user enablement: deliver process/system/tool trainings; facilita

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