IQ

eCOA Data Specialist

Iqvia Biotech
Bangalore1-6 LPA Posted 25 Jun 2025
FULL TIME
Database Design
Data Validation
Process Improvement

Job Description

  •  Undertake eCOA Data Management activities for assigned studies, with/without supervision.
  • May serve in the role of back-up to a DTL.
  • Perform testing of programming and data transfers.
  • Understand and comply with core operating procedures and working instructions.
  • Meet objectives as assigned and develop and maintain good communications and working relationships within eCOA DM team.
  • Database Design and Maintenance: Create and maintain clinical databases to ensure they are efficient and meet the needs of the clinical trials.
  • Data Querying and Reporting: Manage queries and generate reports for analysis.
  • Data Validation: Analyze and resolve discrepancies from Recon/CTMS inquiries.
  • Study Close-out: Execute end-to-end study close-out activities, include Archival.
  • Identify opportunities to automate and improve data collection and management processes.
  • Qualifications:
  • -Bachelor s degree in pharmacy or equivalent preferred.
  • 3-6 years of direct data management experience, preferably a minimum of 1 year as a CDM project lead.
  • Good to have experience in electronic Clinical Outcome Assessment (eCOA) or Decentralized Clinical Trials (DCT).
  • Advanced proficiency in English, both spoken and written.
  • Advanced skills in computer applications like Microsoft Excel, Word, Outlook, etc.
  • - Advanced understanding of the drug development lifecycle and overall clinical research process.
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