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IQVIA Clinical Data Management Jobs – Bangalore, Hyderabad, Pune, Kochi, Kolkata, Thane

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IQVIA is conducting a Virtual Interview Drive on April 8, 2026, inviting experienced Clinical Data Management (CDM) professionals to join its growing team across India. This is a strong opportunity for candidates with 3โ€“5+ years of experience in clinical data management, EDC systems, and study lifecycle execution to secure a role in one of the worldโ€™s leading CROs.

With hybrid work options and multiple location openings including Bangalore, Hyderabad, Pune, Kochi, Kolkata, and Thane, this hiring drive aligns with the increasing demand for clinical data specialists in Indiaโ€™s pharma and CRO sector.


Job Overview โ€“ Clinical Data Management (CDS/Sr CDC)

  • Role: Clinical Data Management (CDS / Sr Clinical Data Coordinator)
  • Experience: 3+ years (4+ preferred)
  • Work Mode: Hybrid
  • Locations: Bangalore, Hyderabad, Pune, Kochi, Kolkata, Thane
  • Interview Mode: Virtual
  • Drive Date: April 8, 2026
  • Last Date to Apply: April 11, 2026

This role focuses on delivering high-quality clinical data management outputs, ensuring compliance, accuracy, and efficiency across clinical trials.


Key Responsibilities

  • Serve as Data Operations Coordinator (DOC) for assigned protocols
  • Perform clinical data review and discrepancy management
  • Write, track, and resolve data clarification forms (DCFs)
  • Support database design, testing, and edit checks
  • Conduct clinical coding (MedDRA/WHO Drug)
  • Participate in database audits and quality checks
  • Collaborate with cross-functional teams (biostatistics, clinical ops)
  • Ensure adherence to SOPs, GCP, and regulatory standards
  • Assist in study start-up, conduct, and close-out activities

Required Qualifications

  • Bachelorโ€™s degree in Life Sciences, Pharmacy, Biotechnology, or related field
  • 3โ€“5+ years of end-to-end Clinical Data Management experience
  • Strong expertise in EDC systems:
    • Medidata Rave
    • Veeva Vault CDMS
    • Oracle Inform
  • Knowledge of:
    • Clinical trial lifecycle
    • Medical terminology
    • Data validation and cleaning processes
  • Skills:
    • Excellent communication
    • Attention to detail
    • Problem-solving and analytical thinking

Preferred Skills

  • Exposure to central lab data handling
  • Experience in database testing and UAT
  • Leadership exposure (backup DOC/DTL roles)
  • Understanding of CDISC standards (SDTM/ADaM)

Salary & Benefits (Estimated)

  • Salary Range: โ‚น6 LPA โ€“ โ‚น12 LPA (based on experience and role level)
  • Hybrid work flexibility
  • Global exposure in clinical trials
  • Career growth in a leading CRO
  • Learning & development programs
  • Health and insurance benefits

Why Join IQVIA?

IQVIA is a globally recognized leader in clinical research, healthcare analytics, and real-world evidence solutions. Working here provides:

  • Exposure to global clinical trials and regulatory environments
  • Opportunity to work with advanced EDC technologies
  • Strong career progression in clinical data management domain

How to Apply

Interested candidates can apply through the following:

Mention subject: Application for Clinical Data Management Role

Application Link

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