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Clinical Database Programmer - Custom Function

TCS
2-5 years
INR 8 LPA – 16 LPA
Mumbai, India
1 June 15, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding

Clinical Database Programmer – Custom Function

Location: Mumbai, Maharashtra, India
Employment Type: Full-Time

Job Summary

The Clinical Database Programmer – Custom Function is responsible for supporting clinical trial data management and clinical database activities across the clinical development lifecycle. The role involves working with clinical trial systems, regulatory standards, and cross-functional stakeholders to ensure high-quality clinical data collection, integration, reporting, and compliance with industry regulations.


Key Responsibilities

Clinical Database Development & Management

  • Support the design, development, configuration, and maintenance of clinical databases for clinical studies.

  • Ensure clinical data systems are configured according to study requirements and regulatory standards.

  • Maintain data integrity, consistency, and quality throughout the clinical trial lifecycle.

  • Participate in database validation, testing, and deployment activities.

Clinical Data Standards & Compliance

  • Apply industry standards including SDTM and ADaM to support clinical data management and reporting activities.

  • Ensure compliance with GxP, HIPAA, and other applicable regulatory requirements.

  • Support data standardization and quality control initiatives across studies.

  • Maintain audit-ready documentation and system records.

Clinical Trial Systems Integration

  • Collaborate with owners of EDC, CTMS, Safety, Data Warehouse, and related clinical systems.

  • Support integration and data flow between clinical trial platforms.

  • Identify system dependencies and ensure alignment across clinical applications.

  • Assist in troubleshooting and resolving data-related issues.

Business Analysis & Requirements Gathering

  • Lead discussions with business stakeholders to understand clinical process requirements.

  • Gather, document, analyze, and validate business requirements.

  • Translate business needs into functional and technical specifications.

  • Collaborate with product teams to ensure successful implementation of requirements.

Biostatistics & Reporting Support

  • Support clinical reporting activities and data outputs required for statistical analysis.

  • Demonstrate understanding of Tables, Listings, and Figures (TLF) generation processes.

  • Collaborate with biostatistics and data management teams to support study deliverables.

  • Ensure reporting requirements are accurately captured and implemented.

Stakeholder Management & Collaboration

  • Act as a liaison between business users, clinical operations teams, and technical teams.

  • Facilitate meetings and discussions with sponsors, study teams, and system owners.

  • Provide updates on project progress, risks, and deliverables.

  • Support continuous process improvement initiatives within clinical data operations.


Required Qualifications

Education

  • Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Clinical Research, Biotechnology, Computer Science, or a related discipline.

Experience

  • 2–6 years of experience in Clinical Data Management, Clinical Database Programming, Clinical Systems, or Clinical Research Operations.

  • Experience supporting clinical trials within pharmaceutical, biotechnology, CRO, or healthcare organizations.

  • Experience working with clinical trial systems and data standards.

Technical Skills

  • Strong understanding of clinical trial operations and data management processes.

  • Knowledge of clinical trial systems such as EDC, CTMS, Safety Systems, and Data Warehouses.

  • Familiarity with SDTM and ADaM standards.

  • Understanding of TLF generation and biostatistics workflows.

  • Knowledge of regulatory requirements including GxP and HIPAA.

  • Experience in requirement gathering, documentation, and system validation.