Clinical Data Services Associate – Medical Monitoring
Location: Bengaluru, India
Job Type: Full-Time
Experience Required: 1–3 Years
Job ID: AIOC-S01619664
Category: Clinical Data Services | Life Sciences R&D
About Accenture
Accenture is a global professional services organization with leading capabilities in digital, cloud, and security. With unmatched experience across more than 40 industries, Accenture delivers Strategy & Consulting, Technology, Operations, and Accenture Song services through the world’s largest network of Advanced Technology and Intelligent Operations centers.
With over 699,000 professionals serving clients in more than 120 countries, Accenture combines technology and human ingenuity to drive innovation, efficiency, and measurable outcomes across industries, including life sciences and healthcare.
Role Overview
The Clinical Data Services Associate will be part of Accenture’s Life Sciences R&D vertical, supporting clinical trial operations through high-quality clinical data services and medical monitoring activities. This role focuses on ensuring data accuracy, compliance, and safety oversight across clinical studies, enabling biopharmaceutical companies to make informed, patient-centric decisions.
The position is ideal for pharmacy and engineering graduates with early-career experience in clinical data management, medical monitoring, or clinical trial support.
Key Responsibilities
Support clinical data services activities across ongoing clinical trials
Manage, process, and validate clinical trial data to ensure accuracy, integrity, and compliance
Provide medical and scientific support for trial oversight and safety-related concerns
Create, review, and validate protocol requirement specifications in alignment with applicable SOPs
Assist in data collection, data cleaning, validation, storage, and analysis activities
Ensure clinical data supports evaluation of safety and efficacy of investigational products
Work with internal teams to resolve routine data or process-related issues using standard guidelines
Utilize clinical systems and tools to manage trial data efficiently
Adhere to regulatory requirements, quality standards, and internal operating procedures
Skills & Competencies
Strong analytical and problem-solving abilities
Adaptable and flexible approach in a dynamic clinical research environment
Basic understanding of clinical trial processes and medical monitoring concepts
Ability to follow standard operating procedures and structured workflows
Good communication and collaboration skills
Willingness to work in rotational shifts, if required
Education & Experience Requirements
BE / Bachelor of Pharmacy / Master of Pharmacy
1 to 3 years of experience in clinical data services, clinical research, medical monitoring, or related life sciences roles
Exposure to clinical trial data management systems and regulatory environments is preferred
Work Structure
Individual contributor role with a focused and predefined scope of work
Tasks performed under detailed to moderate supervision
Primary interaction with immediate team members and reporting supervisors
Decisions primarily impact individual work deliverables
Why Join Accenture?
Work with a global leader in life sciences and healthcare services
Gain exposure to end-to-end clinical research and data services
Build a strong foundation in clinical data management and medical monitoring
Access structured learning, training programs, and long-term career growth opportunities
Be part of a collaborative, innovation-driven, and patient-focused environment
SEO & GEO Optimized Keywords
Clinical Data Services Jobs Bengaluru, Medical Monitoring Jobs India, Clinical Research Associate India, Pharmacy Jobs in Clinical Trials, Accenture Life Sciences Careers, Clinical Data Management Jobs India.
Equal Opportunity Statement
Accenture is an Equal Opportunity Employer. All employment decisions are made without regard to race, religion, gender, sexual orientation, age, disability, or any other legally protected status.
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