Associate Database Programmer
Company: Elanco
Location: Bangalore, Karnataka, India
Job Type: Full-Time
Department: Clinical Data Management / R&D
Experience: 1–4 Years
About the Role
Elanco is seeking an Associate Database Programmer to support global clinical data management operations by designing, developing, validating, and maintaining clinical trial databases. The role involves working closely with Data Management, Biostatistics, Clinical Operations, and Quality teams to ensure high-quality, compliant, and reliable clinical data collection systems.
The successful candidate will contribute to database build activities, electronic data capture (EDC) systems management, validation processes, dashboard development, and continuous improvement initiatives supporting global R&D programs.
Key Responsibilities
Clinical Database Development
Design, develop, validate, and maintain clinical trial databases.
Build and configure database objects, forms, edit checks, and procedures.
Customize forms and edit checks from global libraries according to study specifications.
Ensure consistency and compliance across database builds.
EDC Systems Management
Support deployment, validation, testing, and implementation of Electronic Data Capture (EDC) systems.
Perform User Acceptance Testing (UAT) for system upgrades and new releases.
Troubleshoot database and system-related issues.
Provide ongoing user support and maintenance.
Database Validation & Quality Control
Perform self-testing and quality review of database builds.
Conduct impact assessments for migrations and post-production changes.
Ensure data integrity, validation, and regulatory compliance.
Support quality assurance and audit readiness activities.
Clinical Data Management Support
Maintain Case Report Forms (CRFs) and database structures.
Collaborate with Data Managers, Biostatisticians, Clinical Scientists, and Quality teams.
Support clinical data collection processes and standards.
Contribute to SOPs, QMS documents, and process improvements.
Reporting & Analytics
Develop dashboards and tracking tools for clinical data management activities.
Generate reports to monitor study progress and data quality metrics.
Support data visualization and operational reporting initiatives.
Required Qualifications
Education
Bachelor's Degree in:
Information Technology
Computer Science
Statistics
Life Sciences
Pharmacy
Biotechnology
Related Scientific or Technical Discipline
Experience
Experience in:
Clinical Data Management
Database Programming
Electronic Data Capture (EDC) Systems
Clinical Research Operations
Clinical trial database experience preferred.
Required Skills
Clinical Data Management (CDM)
Database Programming
Electronic Data Capture (EDC)
Clinical Trial Databases
Case Report Forms (CRFs)
Edit Check Programming
Database Validation
User Acceptance Testing (UAT)
Data Integrity
Clinical Research
Dashboard Development
Quality Management Systems (QMS)
SOP Development
Troubleshooting
Stakeholder Collaboration
Preferred Qualifications
Experience with:
Medidata Rave
Oracle Inform
Veeva EDC
Medrio
Other Clinical Trial Database Platforms
Understanding of regulatory requirements for clinical data.
Experience supporting clinical trial studies and study builds.
Knowledge of clinical data standards and validation practices.
Uttar Pradesh :
Agra | Gajraula | Gautam buddha Nagar | Ghaziabad | Gorakhpur | Greater Noida | Jhansi | kanpur | Lucknow | Mathura | Noida | Park City | Prayagraj | Satyamev | Varanasi |Gujarat :
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Hajipur | Patna |Kerala :
Kannur | Kochi | Malappuram | Thiruvananthapuram | Trivandrum |Pondicherry (Puducherry) :
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Remote, India | Siliguri |Illinois :
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Peru | Argentina |Brazil :
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Koropi | Athens |Greece :
Greece |North Island :
Auckland |New Zealand :
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Croatia |Zagreb :
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Tartu | Estonia |Harju County (Maakond) :
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