Location: Bengaluru, India
Company: Accenture
Job ID: AIOC-S01640055
Employment Type: Full-Time
Experience Required: 0–2 years (Freshers can apply)
About the Company
Accenture is a leading global professional services organization with expertise in digital, cloud, and security. With operations across 120+ countries and a workforce of over 700,000 professionals, Accenture delivers integrated solutions across Strategy, Consulting, Technology, and Operations. The company’s Life Sciences R&D division supports end-to-end clinical research, pharmacovigilance, and regulatory services for global biopharma clients.
Job Overview
The Clinical Data Services Associate role is an entry-level opportunity within the Life Sciences R&D vertical, focusing on clinical data management and database programming. The role involves managing, validating, and analyzing clinical trial data to ensure accuracy, regulatory compliance, and high-quality outputs that support drug development and patient safety.
Key Responsibilities
Perform clinical data management activities including data collection, validation, and reconciliation
Develop and review edit checks, patient profiles, and clinical data listings
Work with clinical databases and Electronic Data Capture (EDC) systems
Conduct preprocessing checks and dataset mapping based on study protocols
Utilize tools such as SAS, Cognos, J-Review, or other clinical data platforms
Ensure data integrity, consistency, and compliance with regulatory standards
Collaborate with cross-functional teams including clinical, pharmacovigilance, and regulatory units
Support clinical trial data analysis for safety and efficacy evaluation
Required Skills and Competencies
Strong understanding of Clinical Data Management principles
Knowledge of Clinical Database Testing and EDC Build/Design
Familiarity with clinical trial processes and data lifecycle
Ability to manage multiple stakeholders and communicate effectively
Problem-solving skills with attention to detail
Ability to build and maintain professional client relationships
Roles and Work Structure
Handle routine clinical data tasks based on defined guidelines and SOPs
Work closely with team members and reporting managers
Receive structured training and task-based instructions
Contribute as an individual team member with defined responsibilities
Work in rotational shifts as per project requirements
Educational Qualification
BE or MSc in Life Sciences, Pharmacy, Biotechnology, or related field
Why This Role is Important for Freshers
This position is ideal for candidates starting their career in Clinical Research, Clinical Data Management, or Pharmacovigilance. It provides hands-on exposure to real-world clinical trial data, industry-standard tools, and global regulatory practices—making it a strong foundation for long-term growth in the pharma and CRO industry.
How to Apply
Apply through official company career portals or trusted platforms. For more verified global opportunities in Clinical Research, Pharmacovigilance, and Data Management, visit ThePharmaDaily.com
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