Clinical Data Services Associate
Location: Bengaluru, India
Job Type: Full-Time
Job ID: AIOC-S01626916
Department: Life Sciences R&D – Clinical Data Management
Experience Required: 0–3 Years
Job Overview
Accenture is seeking a Clinical Data Services Associate to join its Life Sciences Research and Development division. This role focuses on clinical data management and clinical database development for global biopharmaceutical clients, supporting clinical trial operations through electronic data capture (EDC) systems and clinical database programming.
The position is suitable for early-career professionals with technical expertise in programming, database development, and clinical trial data processes who want to contribute to clinical research innovation and patient-focused healthcare solutions.
Key Responsibilities
Develop and maintain clinical study databases using Electronic Data Capture (EDC) platforms.
Build electronic Case Report Forms (CRFs) and implement edit and validation checks based on study specifications.
Support updates and modifications to clinical study databases, including protocol amendments through change control processes.
Program data validation rules using Java, JavaScript, SQL, and PL/SQL.
Support integration of data from external sources such as laboratories and Interactive Response Technology (IRT) systems.
Ensure compliance with regulatory standards, data quality requirements, and data security protocols.
Assist in improving database processes, tools, and operational efficiency using industry best practices.
Resolve routine technical and operational issues following standard guidelines and procedures.
Collaborate with team members and supervisors to complete assigned tasks within defined timelines.
Educational Qualifications and Experience Required
Bachelor’s degree in Engineering or Technology (BE/BTech), preferably in Computer Science or related discipline.
0–3 years of experience in clinical data management, clinical database programming, or EDC build activities.
Fresh graduates from 2025 or 2026 batches may apply (all semester results must be available).
Proficiency in English communication required.
Technical Skills and Competencies
Knowledge of clinical data management and clinical trial processes.
Programming experience in Java and JavaScript.
Strong understanding of SQL and Oracle PL/SQL.
Experience in clinical database programming and validation checks.
Strong problem-solving and analytical skills.
Ability to work under pressure and manage multiple priorities.
Adaptability, quick learning ability, and teamwork orientation.
Understanding of regulatory compliance and data quality standards in clinical research.
Work Environment and Role Structure
Individual contributor role within a structured team environment.
Work based on predefined processes and operational guidelines.
Interaction primarily with immediate team members and supervisors.
Role may require working in rotational shifts.
Uttar Pradesh :
Agra | Gajraula | Gautam buddha Nagar | Ghaziabad | Gorakhpur | Greater Noida | Jhansi | Lucknow | Mathura | Noida | Park City | Prayagraj | Satyamev | Varanasi |Gujarat :
Ahmedabad | Ankleshwar | Baroda | Bharuch | Gandhinagar | Gujarat | Halol | Jhagadia | Mehsana | surat | Tarasadi | Vadodara | Vapi |Maharashtra :
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Tartu | Estonia |Harju County (Maakond) :
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