Clinical Data Services Associate (Medical Monitoring)
Job No.: AIOC-S01647299
Location: Bengaluru, India
Company: Accenture
Experience Level: 0–2 years (also listed as 1–3 years)
Qualification: BE / B.Pharm / M.Pharm
Job Overview
The Clinical Data Services Associate works within Life Sciences R&D operations, focusing on clinical data management and medical monitoring support. The role involves handling clinical trial data processing, validation, and quality checks to ensure accuracy, regulatory compliance, and reliability of clinical research data.
This position supports pharmaceutical clients in improving clinical trial outcomes through structured data handling and medical oversight activities.
Key Responsibilities
A. Clinical Data Management
Manage and process clinical trial data from multiple sources
Perform data collection, validation, storage, and quality checks
Ensure accuracy and integrity of clinical trial datasets
Support clinical study teams with structured data workflows
B. Medical Monitoring Support
Provide medical oversight support for clinical trials
Assist in reviewing protocol requirements and study specifications
Support safety-related concerns in collaboration with clinical teams
Contribute to validation of protocol requirement specifications
C. Data Quality & Compliance
Ensure clinical data meets applicable SOPs and regulatory standards
Support compliance with clinical trial quality requirements
Assist in identifying and resolving routine data issues
D. Systems & Tools
Work with specialized clinical data management systems
Support efficient handling of trial data using enterprise tools
Maintain structured documentation of data processes
E. Team Support & Operations
Work as an individual contributor within a team
Follow detailed instructions for assigned tasks
Support supervisor and team leads in daily operations
Work in rotational shifts if required
Core Skills Required
Clinical data management
Basic understanding of clinical trials
Medical monitoring support
Data validation and quality control
SOP-based documentation practices
Communication and coordination skills
Problem-solving in structured workflows
Soft Skills
Adaptability and flexibility
Attention to detail
Basic analytical thinking
Communication (written and verbal)
Ability to follow structured instructions
Work Environment
Clinical R&D operations environment
Entry-level / trainee-style structured role
Rotational shift-based global support function
Process-driven work with strict SOP adherence
Career Positioning Insight
This is an entry-level clinical operations / data services role, typically a starting point into:
Clinical Data Management
Clinical Operations (CRA track)
Pharmacovigilance (entry transition possible)
Medical Monitoring / Clinical Research analytics
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