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ICON plc hiring Clinical Trial Assistant (CTA)

Published on

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences

Mumbai, India (Office-based)

1–2 years

Verified Job

Online Application

Global CRO leader ICON plc is hiring a Clinical Trial Assistant (CTA) for its Mumbai office (office-based role). This opportunity is ideal for professionals with 1–2 years of experience in global clinical trials, TMF management, and regulatory documentation.

If you have hands-on exposure to Veeva Vault, CTMS, EDC systems, and strong knowledge of ICH-GCP guidelines, this Clinical Trial Assistant job in Mumbai could accelerate your clinical research career.


📌 Job Overview – Clinical Trial Assistant (CTA)

  • Company: ICON plc
  • Role: Clinical Trial Assistant (CTA)
  • Location: Mumbai, India (Office-based)
  • Experience: 1–2 Years
  • Domain: Oncology, Cardiology, Pulmonology, Immunology Trials
  • Job Type: Full-Time

This Clinical Trial Assistant role supports global clinical operations, ensuring documentation accuracy, regulatory compliance, and inspection readiness.

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🔎 Key Responsibilities – Clinical Trial Assistant

As a CTA at ICON, you will:

  • Support global study teams with Trial Master File (TMF) maintenance
  • Manage and update Veeva Vault, CTMS, and EDC platforms
  • Assist in Ethics Committee (EC) submissions and Health Authority (HA) submissions
  • Track essential documents and clinical trial milestones
  • Coordinate meetings, training documentation, and trial communications
  • Support site start-up activities and document collection
  • Maintain inspection-ready documentation for audits
  • Liaise with vendors, internal teams, and site staff

This Clinical Trial Assistant job requires precision in documentation and adherence to global regulatory frameworks.

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🎓 Qualifications & Skills Required

To qualify for this Clinical Trial Assistant position:

  • 1–2 years of experience as a Clinical Trial Assistant (CTA)
  • Hands-on experience in:
    • EC & HA submissions
    • Site payments tracking
    • Essential clinical trial documentation
  • Strong understanding of ICH-GCP and global clinical operations
  • Proficiency in:
    • Veeva Vault
    • CTMS systems
    • EDC platforms
  • Excellent organizational and communication skills
  • Ability to work in a fast-paced global CRO environment

💰 Salary & Benefits

Estimated Salary Range: ₹4.5 – ₹6.5 LPA (based on industry standards for CTA roles in Mumbai)

ICON offers:

  • Competitive salary structure
  • Health insurance coverage
  • Retirement planning benefits
  • Life assurance
  • Global Employee Assistance Programme (TELUS Health)
  • Work-life balance initiatives
  • Inclusive and diverse workplace culture

🌍 Why Choose ICON?

ICON plc is a globally recognized clinical research organization known for excellence in healthcare intelligence and clinical development.

Working as a Clinical Trial Assistant at ICON provides exposure to:

  • Global oncology and cardiology trials
  • Advanced clinical systems (Veeva Vault, CTMS, EDC)
  • International regulatory standards
  • Structured CRO workflows

This role strengthens your foundation for future growth into Clinical Research Associate (CRA), Study Coordinator, or Clinical Project roles.


📝 How to Apply

Application Link

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