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Clinical Data Svs Associate

Accenture
Accenture
1-3 years
Not Disclosed
Bengaluru, India
10 March 24, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Data Services Associate

Location: Bengaluru
Job Type: Full-Time
Experience Required: 1–3 years
Job ID: AIOC-S01633225

Overview
Join Accenture as a Clinical Data Services Associate within the Life Sciences R&D division. This role offers an opportunity to contribute to high-impact clinical research projects by ensuring the integrity, accuracy, and compliance of clinical trial data. You will support global biopharma clients in delivering safe and effective treatments through robust data management and eTMF processes.

Key Responsibilities
Manage and support clinical data services activities, including eTMF (electronic Trial Master File) management and documentation processes aligned with global regulatory standards
Perform data validation, quality checks, and reconciliation of clinical trial documents to ensure completeness and accuracy
Conduct format and compliance checks for documents to meet eCTD submission standards, including PDF properties, bookmarks, and hyperlink validation
Support lifecycle management of clinical trial documentation, including protocol packages, amended checklists, and end-of-trial documentation
Assist in clinical study report appendices preparation and essential document tracking
Collaborate with cross-functional stakeholders to ensure timely and high-quality deliverables
Ensure adherence to Good Documentation Practices (GDP) and regulatory requirements

Required Skills and Competencies
Strong understanding of clinical data management and eTMF processes
Ability to manage multiple stakeholders and meet strict deadlines
Excellent attention to detail and quality-focused mindset
Strong communication and client relationship management skills
Ability to work under pressure in a fast-paced environment

Eligibility Criteria
Master’s degree (MSc) in Life Sciences or a related field
1–3 years of experience in clinical data management, eTMF, or related domains

About the Company
Accenture is a leading global professional services firm specializing in digital, cloud, and security solutions. With operations in over 120 countries and a workforce of more than 700,000 professionals, Accenture delivers innovative solutions across Strategy, Consulting, Technology, and Operations. The Life Sciences R&D vertical focuses on accelerating clinical development, regulatory compliance, and patient-centric innovation.

Why Apply
Opportunity to work on global clinical research projects
Structured learning and career growth in clinical data and regulatory domains
Exposure to advanced technologies and global best practices in life sciences

Work Environment
This role may require working in rotational shifts based on business requirements and project timelines.