Job Title: Specialist I – Global Clinical Solutions
Location: Bangalore, India
Company: AstraZeneca
Employment Type: Full-Time
Job Requisition ID: R-246692
Application Deadline: April 3, 2026
Experience Required: 3–6 Years (Clinical Systems / Clinical Coding / Study Delivery Support)
Specialist I – Global Clinical Solutions | Clinical Systems & Coding Expert
AstraZeneca is hiring a Specialist I – Global Clinical Solutions to support global clinical trial delivery through robust clinical systems management, coding excellence, and first-line user support. This role plays a critical part in ensuring data integrity, study delivery efficiency, and seamless clinical operations across global programs.
This opportunity is ideal for professionals with hands-on experience in clinical coding, study delivery systems, regulatory compliance, and cross-functional clinical support within a global pharmaceutical or CRO environment.
Role Overview
The Specialist, Global Clinical Solutions will act as a key operational partner to study teams by maintaining core study delivery systems, supporting financial and compliance processes, and ensuring high-quality clinical coding using standardized medical dictionaries.
The role bridges clinical operations, data management, and system governance, enabling faster study decisions, regulatory readiness, and consistent global execution.
Key Responsibilities
Study Delivery Systems Stewardship
Maintain and monitor systems related to:
Financial Disclosure
Drug Return and Destruction
Pairs Investigator Database
Investigator Safety Letter Distribution
Clinical Trial Registration
Ensure high standards of data integrity, quality, and consistency across global study delivery platforms.
First-Line User Support
Provide timely first-line support for study delivery systems.
Troubleshoot system issues and guide users to ensure uninterrupted study execution.
Monitor system data integrity and escalate critical issues as per established processes.
Clinical Coding & Data Quality
Perform accurate and consistent clinical coding or review CRO-coded data including:
Medical history
Surgical history
Adverse events
Concomitant medications
Use agreed versions of clinical coding dictionaries (e.g., MedDRA, WHO Drug) and follow global coding guidelines.
Raise and resolve coding queries according to study timelines and regulatory requirements.
Monitor and respond to coding-related Global Data Management Requests (GDMRs) and escalate to GCDMT where required.
Financial & Operational Support
Process financial charges related to study delivery support activities.
Ensure alignment between operational data and financial tracking systems.
Project & Non-Drug Proposal Support
Contribute to development of business cases supporting prioritization of non-drug project proposals.
Link operational system improvements to measurable study delivery value.
Knowledge Sharing & Continuous Improvement
Collaborate with cross-functional clinical development, operations, and data teams.
Develop and maintain communication tools supporting study delivery.
Support global integration and standardization of systems and services.
Identify opportunities for scalability and operational efficiency.
Safety, Health & Environment (SHE) Compliance
Adhere to global SHE standards and legal compliance requirements.
Promote responsible system and data management practices.
Essential Qualifications & Experience
3–6 years of experience in Clinical Operations, Clinical Data Management, Clinical Coding, or Study Delivery Support.
Hands-on experience maintaining clinical study systems.
Proficiency in coding clinical study data using MedDRA and WHO Drug dictionaries.
Experience raising and resolving coding queries within global processes.
Strong understanding of data integrity principles and regulatory compliance.
Experience processing financial activities linked to study operations.
Strong written and verbal communication skills.
Preferred Qualifications
Experience supporting prioritization of non-drug or operational improvement initiatives.
Exposure to global clinical development environments.
Demonstrated ability to work across multicultural teams.
Strong analytical thinking and problem-solving capability.
Proven ability to manage multiple priorities in fast-paced clinical environments.
Work Model
This position follows a hybrid work structure with an average expectation of three days per week in the office, balancing collaboration and flexibility.
Why Join AstraZeneca
AstraZeneca is a global biopharmaceutical leader committed to advancing science and delivering life-changing medicines. By combining scientific expertise with advanced digital, data science, and AI capabilities, AstraZeneca accelerates clinical development while maintaining the highest standards of data integrity and patient safety.
This role offers the opportunity to contribute to global clinical trial excellence, work with cross-functional experts, and directly impact the speed and quality of clinical decision-making worldwide.
Diversity & Inclusion Statement
AstraZeneca is committed to fostering an inclusive and diverse work environment. Applications are welcomed from qualified candidates of all backgrounds, in compliance with applicable employment laws and equal opportunity regulations.
If you are a clinical systems and coding professional looking to contribute to global trial efficiency and regulatory excellence, apply now to join AstraZeneca’s Global Clinical Solutions team in Bangalore.
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