Clinical Data Services Associate | Clinical Data Management | Bengaluru
Company: Accenture
Location: Bengaluru
Job Type: Full-Time
Work Mode: On-site
Experience: 0–2 Years
Qualification: Bachelor of Pharmacy (B.Pharm)
Job Overview
This role is an excellent entry point into the clinical research and data management domain, where you will work on clinical trial data processing, validation, and quality control.
As a Clinical Data Services Associate, you will support global clinical trials by ensuring accurate, reliable, and regulatory-compliant data handling, which is critical for evaluating the safety and efficacy of drugs and medical treatments. This position sits at the intersection of clinical research, pharmacovigilance, and regulatory operations, making it highly valuable for long-term career growth in pharma.
Key Responsibilities
Clinical Data Management
Manage and process clinical trial data across multiple studies
Perform data collection, validation, and quality checks
Ensure data accuracy for clinical research and regulatory submissions
Data Quality & Compliance
Maintain high standards of data integrity and consistency
Ensure compliance with GCP, regulatory guidelines, and sponsor requirements
Support data cleaning, discrepancy management, and query resolution
Clinical Trial Support
Assist in data integration, storage, and analysis processes
Work with cross-functional teams in clinical, PV, and regulatory domains
Support end-to-end clinical trial data lifecycle
Stakeholder & Process Coordination
Collaborate with internal teams and stakeholders for timely data delivery
Handle multiple projects and deadlines efficiently
Build and maintain strong client relationships
Required Skills & Qualifications
Education & Experience
Bachelor of Pharmacy (B.Pharm) required
1–3 years of experience in clinical data management / life sciences domain
Core Technical Skills
Knowledge of:
Clinical Data Management (CDM)
Clinical Trial Processes (Phase I–IV)
Data Validation & Data Cleaning
Familiarity with:
ICH-GCP Guidelines
Clinical trial databases / EDC systems
Regulatory compliance standards
Soft Skills
Strong analytical and problem-solving skills
Ability to manage multiple stakeholders and deadlines
High attention to detail and data accuracy focus
Ability to work under pressure in a fast-paced environment
Perks & Benefits
Opportunity to work in global clinical research & pharma projects
Strong career pathway into Clinical Data Management, Pharmacovigilance, and Regulatory Affairs
Access to learning platforms and certification programs
Exposure to international clinical trial standards and systems
Inclusive and growth-oriented workplace
About the Company
Accenture is a global leader in digital, consulting, and healthcare services, supporting life sciences organizations across clinical research, pharmacovigilance, and regulatory operations. With a presence in 120+ countries, Accenture drives innovation and efficiency in healthcare delivery.
Salary / Compensation
💰 Not disclosed in the job description (Competitive entry-level package expected)
Work Mode
📍 On-site – Bengaluru, India
Call to Action
If you want to build a strong foundation in clinical data management, clinical trials, and pharma R&D operations, this role offers the right exposure and growth.
👉 Apply now and kickstart your career in clinical research and data management.
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