Specialist, Global Clinical Solutions – Bengaluru, India
Job Type: Full-Time | Experience Required: 5+ Years | Job Requisition ID: R-244387
About the Role
AstraZeneca is seeking a Specialist in Global Clinical Solutions to support the delivery of clinical studies with precision, speed, and integrity. This role bridges clinical operations, data management, and coding systems, ensuring that study teams can make informed decisions and advance medicines to patients efficiently.
You will manage critical clinical systems, safeguard data quality, provide first-line user support, and contribute to process improvements. Your work will directly impact the accuracy of clinical data, the efficiency of study delivery, and the scalability of global trials.
Key Responsibilities
Clinical Systems & Study Support:
Maintain systems related to Financial Disclosure, Drug Return & Destruction, Pairs Investigator Database, Investigator Safety Letter Distribution, and Clinical Trial Registration, ensuring consistency and compliance.
Provide first-line support to system users, resolving issues and guiding study teams effectively.
Monitor data integrity and process financial charges linked to study delivery activities.
Clinical Coding & Data Management:
Perform accurate and consistent hands-on coding or review of CRO-coded clinical study data (medical history, surgical history, adverse events, drugs) using approved coding dictionaries and guidelines.
Raise and resolve coding queries according to global and local processes and timelines.
Monitor coding-related GDMRs and escalate to the Global Clinical Data Management Team (GCDMT) as required.
Continuous Improvement & Knowledge Sharing:
Collaborate with cross-functional teams to share protocols, experiences, and best practices.
Support integration and standardization of global clinical systems and services.
Contribute to prioritization of non-drug project proposals, linking investment to measurable study delivery value.
Leadership & Compliance:
Demonstrate ownership, creativity, and collaboration across project activities.
Ensure adherence to Safety, Health, and Environment (SHE) standards and legal obligations.
Promote a culture of courageous leadership, innovation, and collaboration within clinical operations.
Essential Skills & Experience
Clinical, healthcare, or scientific qualification (BSc, MSc, or equivalent).
5+ years of experience in clinical operations, data management, or clinical coding within the pharmaceutical industry.
Strong understanding of clinical study delivery systems and clinical coding dictionaries.
Proficiency in resolving queries, managing data integrity, and financial processing in clinical trial systems.
Ability to collaborate across global matrix teams and manage multiple priorities simultaneously.
Excellent written and verbal communication skills for cross-functional and international stakeholders.
Preferred Skills
Experience in non-drug project prioritization and system integration projects.
Knowledge of global and local clinical trial standards, GCP guidelines, and regulatory expectations.
Demonstrated ability to foster innovation, process improvement, and team knowledge sharing.
Why Join AstraZeneca?
At AstraZeneca, scientific curiosity meets practical delivery. You will partner with clinicians, data experts, and operators to push boundaries, supported by digital, AI, and data-driven technologies. You will contribute to faster, safer, and more efficient clinical studies, impacting patient outcomes worldwide.
We value diversity, inclusion, and collaboration, giving you the freedom to innovate, challenge assumptions, and advance clinical research at a global scale.
Location: Bengaluru, India | Work Arrangement: Hybrid (minimum three days in-office per week)
How to Apply
Step into this role to transform clinical data practice into actionable insights, accelerate study delivery, and drive patient impact globally. Submit your application through our online portal before January 29, 2026.
Gujarat :
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Siliguri |Illinois :
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