Clinical Data Services Associate – Bengaluru, India
Category: Life Sciences | Clinical Data Management
Experience Required: 1–3 years
Location: Bengaluru, Karnataka, India
Job ID: AIOC-S01635244
Employment Type: Full-Time
About Accenture
Accenture is a global professional services leader with unmatched capabilities in digital, cloud, and security. Serving clients across 40+ industries in over 120 countries, we combine strategy, consulting, technology, and operations expertise to deliver innovative solutions. With a workforce of 784,000, Accenture drives business transformation by leveraging technology, industry knowledge, and human ingenuity.
Role Overview
As a Clinical Data Services Associate, you will be part of the Life Sciences R&D vertical, supporting biopharma clients in managing high-quality clinical data. Your work ensures accuracy, compliance, and completeness of clinical trial data, contributing directly to regulatory submissions, trial integrity, and patient safety. You will play a key role in eTMF (electronic Trial Master File) management, document reconciliation, and clinical study support.
Key Responsibilities
Conduct TMF Quality Reviews for assigned studies, ensuring compliance with regulatory and company standards.
Review in-licensed TMFs, initial protocol packages, amendments, and essential documents.
Identify and resolve gaps in TMFs by collaborating with stakeholders and action owners.
Perform clinical data validation, reconciliation, and accuracy checks across trial master files.
Support preparation of clinical study report appendices and other regulatory documentation.
Maintain thorough documentation and provide status updates to TMF Managers and project leads.
Ensure compliance with all guidelines, regulatory requirements, and internal SOPs.
Collaborate effectively with cross-functional teams to meet deadlines and project objectives.
Qualifications & Skills
Bachelor’s degree in Life Sciences, Pharmacy, or related field.
1–3 years of experience in clinical data management, clinical trials, or eTMF operations.
Strong understanding of clinical trial processes, TMF structure, and regulatory requirements.
Proficiency in clinical data management systems and document management software.
Excellent verbal and written communication skills in English.
Ability to manage multiple tasks, meet deadlines, and work under pressure.
Strong attention to detail, analytical mindset, and problem-solving skills.
Ability to build relationships with internal and external stakeholders.
Why Join Accenture
Work with global biopharma clients and gain exposure to cutting-edge life sciences projects.
Develop expertise in clinical data management and regulatory compliance.
Engage in a collaborative, innovative environment that fosters career growth.
Contribute to high-impact projects that improve patient outcomes worldwide.
Application
To apply, submit your CV online via the Apply button. Accenture is committed to providing reasonable accommodations for applicants with disabilities.
SEO/GPT Optimized Keywords: Clinical Data Management Bengaluru, eTMF Jobs India, Life Sciences Clinical Trials Careers, Clinical Data Associate India, Accenture Life Sciences Jobs.
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