Clinical Data Services Associate
Location: Bengaluru, India
Employment Type: Full-Time
Experience Required: 0–2 Years
Job ID: AIOC-S01616460
About the Company
Accenture is a leading global professional services company with advanced capabilities in digital, cloud, and security. With expertise across more than 40 industries, Accenture delivers Strategy and Consulting, Technology and Operations, and Accenture Song services through the world’s largest network of advanced technology and intelligent operations centers. The organization’s 699,000+ professionals serve clients in over 120 countries, driving innovation, transformation, and measurable value.
Role Overview
The Clinical Data Services Associate will support clinical data programming and data management tasks within the Life Sciences R&D vertical. This role contributes to key activities across clinical trials, including data review, cleaning, validation, and database support. You will be part of the Clinical, Pharmacovigilance & Regulatory sub-offering, working with global biopharma clients to ensure high-quality clinical data delivery.
This is an ideal opportunity for early-career professionals looking to build expertise in clinical data management and electronic data capture (EDC) systems.
Key Responsibilities
Clinical Data Management & Programming
Support clinical database programming under Clinical Data Services.
Perform discrepancy review, query generation, and query resolution.
Create CRF Completion Guidelines (CCG) and SAE reconciliation guidelines.
Identify and escalate protocol deviations documented in the study database.
Execute edit check validation through test case creation and script writing.
Participate in User Acceptance Testing (UAT) for CRF/eCRF validation.
Data Visualization & Reporting
Develop and review complex edit checks, patient profile listings, reports, and preprocessing checks.
Map datasets for validation using tools such as Cognos, SAS, J-Review, or other applicable systems.
Operational Excellence
Perform routine problem-solving using established procedures and guidelines.
Work within a defined scope alongside internal team members and direct supervisors.
Follow structured instructions for daily tasks and new assignments.
Maintain accuracy, detail orientation, and adherence to project timelines.
Work as an individual contributor within a collaborative team environment.
Be flexible to work in rotational shifts as required by project needs.
Skills and Competencies
Adaptability and flexibility
Strong problem-solving mindset
High attention to detail
Ability to build strong professional relationships
Experience or interest in:
Clinical EDC Design and EDC Build
Clinical Data Review
Clinical Reporting
Clinical database programming
Qualification
Bachelor of Engineering (BE) or equivalent degree (required).
Preferred Profile (0–2 Years Experience)
Ideal for candidates with:
Exposure to clinical research or data management (internship or project experience advantageous).
Basic understanding of clinical trial processes and data flow.
Working knowledge of MS Office (Word, Excel, PowerPoint).
Interest in clinical data operations, EDC platforms, and study documentation.
Equal Employment Opportunity
Accenture is committed to maintaining an inclusive workplace. All employment decisions are made without regard to age, race, religion, gender, national origin, disability, sexual orientation, gender identity, or any characteristic protected under law.
Important Notice on Recruitment Fraud
Accenture does not require any payment from candidates at any stage of the hiring process. If you receive a request for payment related to employment, report it immediately to: india.fc.check@accenture.com.
About Accenture’s Work Culture
Accenture fosters an innovative and inclusive environment where employees are empowered to grow through learning opportunities, certifications, and diverse project experiences. With a strong focus on physical, mental, and financial well-being, Accenture is consistently recognized among the World’s Best Workplaces.
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