Project Title: Database Management Analyst

Work Experience: 2 to 8 Years

Work location: Bengaluru.

Work Mode: Kochi/Bangalore/Mumbai/Kolkata

Must Have Skills: Clinical SAS/DM SAS/SAS Macros/ SAS Programming (clinical)

edit check, listings

Key Responsibilities:
Support Clinical Data Management activities within Biometrics.
Collaborate with programmers, data managers, statisticians, safety, regulatory, and project teams.
Ensure clinical data quality, accuracy, and consistency.
Provide programming support as per study timelines and specifications.
Contribute to data validation and transfer specifications.
Support clinical data reporting and regulatory submissions.
Monitor data quality and resolve study data issues.
Act as Study Clinical Programmer.
Review work completed by supporting programmers.
Attend study team meetings and provide inputs.




Manage delivery timelines.
Perform ETL (Extract, Transform, Load) of clinical data.
Generate edit checks, listings, and reports.
Execute assigned study-related tasks.

Qualifications & Skills
Bachelor's degree in Mathematics, Computer Science, or equivalent.
Solid verbal and written communication skills.
Knowledge of pharmaceutical clinical development and regulatory submissions.
Understanding of statistical concepts and techniques.
Experience with clinical data development, validation, and documentation.
Knowledge of FDA 21 CFR Part 11, EDC, and Clinical Data Management systems.
Understanding of clinical studies; biomarker data experience is preferred.

📌 Database Management Analyst Bengaluru (India)
🏢 Iqvia
📍 India