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Tier-1 pharma brand, Bangalore location, and mid-level data role create moderate applicant competition.
Clinical trial data, EDC/CDMS experience and regulatory/GCP familiarity limit cross-industry transferability.
Requires 2+ years clinical DM experience, pharma systems (EDC/CDMS), and UAT/validation skills, making filters moderately strict.
Lead planning and execution of clinical data review and risk-based data management activities ensuring high quality data for analysis and regulatory submission.
Develop and specify data review tools including reports and visualizations; collaborate with programmers for deployment and perform detailed data integrity checks across datasets, listings, and analytics.
Communicate data insights clearly to stakeholders, support operational decision-making, and maintain trial documentation including preparation for audits and inspections.
Bachelor's or Master's degree in Natural/Life Science, Medicine, or Computer Science with equivalent professional experience.
Preferably 2+ years of Clinical Data Management experience, mostly within pharmaceutical industry or drug development.
Knowledge of clinical trial methodology and a basic understanding of GCP and relevant regulatory requirements.
Work Experience Required: Preferably 2+ years in Clinical Data Management; Notice Period: Not explicitly mentioned in the JD.
Experienced in clinical data review within pharmaceutical drug development and familiar with clinical trial data processing and systems.
Skilled in data visualization and analytical methods to identify data patterns, anomalies, and support risk management.
Effective communicator comfortable coordinating across global teams and maintaining relationships with multiple stakeholders in a structured, regulated environment.