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IQVIA Hiring For Clinical Data Management Professional

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Are you an experienced Clinical Data Management professional looking for your next career move in the pharmaceutical and clinical research industry? IQVIA is conducting a walk-in interview for Clinical Data Management professionals on 27th February 2026 (Friday) at its Thane office.

This opportunity is ideal for candidates with 4+ years of Clinical Data Management experience, strong expertise in Veeva EDC, and hands-on exposure to end-to-end clinical data management processes across the study lifecycle.

If you are seeking Clinical Data Management jobs in Thane or exploring CRO career opportunities in India, this hiring drive could be your next big step.


📅 Walk-In Interview Details

  • Position: Clinical Data Management Professional
  • Experience Required: Minimum 4 years
  • Interview Date: 27th February 2026 (Friday)
  • Location: Thane, Maharashtra
  • Mode: Walk-In Interview

🔍 Key Responsibilities – Clinical Data Management

Selected candidates for the Clinical Data Management role will be responsible for:

  • Managing end-to-end Clinical Data Management processes
  • Supporting clinical trial start-up, conduct, and close-out activities
  • Designing and reviewing eCRFs (electronic Case Report Forms)
  • Performing data validation, discrepancy management, and query resolution
  • Ensuring compliance with ICH-GCP guidelines and regulatory standards
  • Coordinating with cross-functional teams including Clinical Operations, Biostatistics, and Medical Writing
  • Maintaining data integrity in Veeva and Veeva EDC platforms
  • Contributing to database lock and study close-out deliverables

This Clinical Data Management job requires strong analytical skills and deep familiarity with clinical trial data workflows.


✅ Qualifications & Skills Required

To qualify for this Clinical Data Management opportunity, candidates should have:

  • Minimum 4 years of relevant industry experience in Clinical Data Management
  • Experience across the full clinical study lifecycle
  • Hands-on expertise in Veeva and Veeva EDC
  • Strong understanding of CDISC standards, GCP, and regulatory requirements
  • Experience working in a CRO or pharmaceutical company
  • Excellent documentation and communication skills

Professionals with prior exposure to global clinical trials and regulatory submissions will have an added advantage.


💼 Why Consider This Clinical Data Management Role?

Working in Clinical Data Management at a leading CRO offers:

  • Exposure to global clinical trials
  • Opportunity to work with advanced Veeva EDC platforms
  • Career growth in the clinical research and pharmaceutical industry
  • Competitive salary structure
  • Professional development and training programs
  • Collaborative and innovation-driven work culture

This role is particularly suitable for professionals seeking Clinical Data Management jobs in Maharashtra or advancement in CRO data management careers.


💰 Salary Range (Indicative)

  • ₹8,00,000 – ₹14,00,000 per annum (INR)
  • Based on experience, expertise in Veeva EDC, and clinical trial exposure

📧 How to Apply

Interested candidates with relevant Clinical Data Management experience can share their updated CV at:

📩 jinto.jacobc@iqvia.com

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