Specialist I, Global Clinical Solutions

Why This Role Matters

The Specialist I, Global Clinical Solutions role at AstraZeneca plays a critical part in ensuring clinical trials run efficiently, accurately, and in compliance with global standards. Behind every successful clinical study is a strong foundation of clean data, reliable systems, and precise clinical coding. This position safeguards that foundation.
By supporting study delivery systems, maintaining coding accuracy, and providing first-line user support, you directly contribute to faster decision-making and smoother trial execution. The impact of this role extends beyond data—it helps accelerate the development of life-changing medicines for patients worldwide.

Job Description

The Specialist, Global Clinical Solutions will support global study teams by maintaining key clinical systems, ensuring data integrity, performing clinical coding activities, and resolving system-related queries. The role combines technical expertise, operational coordination, and user support to ensure global trials operate seamlessly.
The candidate will collaborate across Clinical Development, Data Management, and Operations teams while contributing to process improvements and system integration initiatives.

Key Features of the Role:

• Global clinical trial exposure
• Hands-on clinical coding and system stewardship
• Cross-functional collaboration with study teams
• First-line system and user support responsibilities
• Hybrid work model (minimum three days per week in office)
• Opportunity to contribute to non-drug project proposals

Responsibilities

• Maintain systems related to Financial Disclosure, Drug Return and Destruction, Pairs Investigator Database, Investigator Safety Letter Distribution, and Clinical Trial Registration
• Provide first-line user support for study delivery systems and resolve issues promptly
• Monitor and maintain data integrity within Study Delivery (SD) systems
• Process financial charges associated with study delivery support activities
• Perform accurate clinical coding or review CRO-coded data (medical history, surgical history, adverse events, drugs) using approved coding dictionaries
• Raise, track, and resolve coding-related queries according to global and local study processes
• Monitor and respond to coding-related GDMRs and escalate to the GCDMT when required
• Contribute to development of cases prioritizing non-drug project proposals
• Share knowledge, maintain communication tools, and support global system integration
• Ensure compliance with Safety, Health, and Environment (SHE) standards

Educational Requirements:

• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or a related field

Essential Skills and Experience:

• Experience maintaining clinical study delivery systems
• Strong understanding of clinical coding practices and dictionaries (e.g., MedDRA, WHO Drug)
• Hands-on experience coding clinical study data
• Knowledge of global and local study processes and timelines
• Experience in first-line user support and data integrity monitoring
• Familiarity with financial processing related to study support activities
• Strong attention to detail and analytical skills
• Effective communication and collaboration abilities

Desirable Skills and Experience:

• Experience supporting non-drug project proposal prioritization
• Exposure to global system integration initiatives
• Ability to contribute to continuous improvement strategies
• Leadership mindset with collaborative approach
• Commitment to quality, compliance, and innovation

Important Date

• Closing Date: 03-Apr-2026

Company Overview

AstraZeneca is a global, science-led biopharmaceutical company focused on the discovery, development, and commercialization of prescription medicines. The organization emphasizes innovation, digital transformation, and collaborative science to accelerate drug development and improve patient outcomes worldwide.
With strong investments in data science, AI capabilities, and global collaboration, AstraZeneca fosters a culture of inclusion, scientific curiosity, and operational excellence.

Work Model

The role follows a hybrid working model with an average expectation of a minimum of three days per week in the office, balancing collaboration with individual flexibility.

FAQs

1. What type of role is this?
It is a global clinical operations and systems support role focused on clinical coding and study delivery systems.

2. Is clinical coding experience mandatory?
Yes, hands-on coding or review experience of clinical study data is essential.

3. Where is the job location?
The position is based in Bangalore, India.

4. What is the last date to apply?
The closing date is 03-Apr-2026.

5. Does the role involve cross-functional collaboration?
Yes, the role requires working closely with Clinical Development, Data Management, and Operations teams globally.

Application Tips

• Highlight experience in clinical coding and study systems
• Mention familiarity with coding dictionaries such as MedDRA and WHO Drug
• Demonstrate experience in resolving system queries and supporting users
• Showcase cross-functional collaboration examples
• Apply early to ensure timely consideration