Database Designer – Clinical Trials
Company: Sun pharma
Business Unit: Clinical Research / Data Management
Location: Mumbai, India / Remote (Hybrid options available)
Job Type: Full-Time
Experience Required: 2–5 Years
Posted Date: January 2026
Job Overview
We are seeking an experienced Database Designer – Clinical Trials to join our Clinical Data Management team. The role is responsible for designing, developing, and maintaining clinical trial databases that ensure data integrity, accuracy, and regulatory compliance throughout the study lifecycle. The ideal candidate will have hands-on experience in electronic data capture (EDC) systems, strong understanding of clinical trial processes, and proficiency in database design for multi-center clinical studies.
This position provides an opportunity to work on global clinical trials, collaborate with cross-functional teams, and contribute to high-quality data collection that supports life-changing therapies.
Key Responsibilities
Design and configure clinical trial databases using EDC systems such as Medidata RAVE, Veeva Vault, Oracle Clinical, or equivalent
Develop case report forms (CRFs), edit checks, and data validation plans based on study protocols and regulatory requirements
Collaborate with Clinical Operations, Biostatistics, Data Management, and Medical Writing teams to ensure database design aligns with study objectives
Conduct database testing, validation, and User Acceptance Testing (UAT) to ensure functionality, accuracy, and regulatory compliance
Maintain and update databases throughout the study lifecycle, including amendment implementation and version control
Generate data extracts, datasets, and reports for internal review, regulatory submission, and statistical analysis
Ensure compliance with ICH-GCP guidelines, CDSCO/US FDA/EMA regulations, and internal SOPs
Support training of study teams on database usage, system functionality, and best practices
Identify and resolve system issues, workflow challenges, and data discrepancies in collaboration with IT and study teams
Educational Qualification
Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Computer Science, Information Technology, or related fields
Postgraduate Diploma or Certification in Clinical Data Management / Clinical Research is preferred
Experience Requirements
2–5 years of experience in clinical trial database design and data management
Proven experience in EDC system configuration, CRF design, and clinical data validation
Experience in multi-center, global clinical trials is a strong advantage
Required Skills and Competencies
Strong knowledge of clinical trial processes, GCP, and regulatory compliance
Hands-on experience with database design, edit checks, and UAT
Proficiency in SQL, data management tools, and EDC platforms
Strong analytical, problem-solving, and attention-to-detail skills
Excellent written and verbal communication skills in English
Ability to collaborate with cross-functional teams in a global clinical research environment
Flexibility to adapt to changing project requirements and timelines
Why Join Us?
Join a global pharmaceutical organization where your expertise in clinical trial databases directly contributes to the development of innovative therapies. Benefit from professional growth opportunities, exposure to international clinical trials, and a supportive, collaborative environment that values quality, compliance, and scientific excellence.
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