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Clinical Trial Assistant Job in Romsons

Published on

Romsons

M.Pharm / MSc (Life Sciences or related field)

Noida

1โ€“4 years

Verified Job

Online Application
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Looking to build a career in clinical research and medical devices? A new opportunity is open for a Clinical Trial Assistant (CTA) at Romsons Group of Industries, Noida. This role is ideal for candidates with experience in PMCF, Clinical Evaluation, Vigilance, and Post-Market Surveillance (PMS).

This clinical trial assistant job in Noida offers hands-on exposure to clinical evaluation reports (CER), risk management, and regulatory compliance, making it a strong entry point into medical device clinical research careers.


Key Responsibilities โ€“ Clinical Trial Assistant

As a Clinical Trial Assistant, you will support clinical and regulatory functions across multiple domains:

  • Assist in Post-Market Clinical Follow-up (PMCF) activities
  • Support preparation and updates of Clinical Evaluation Reports (CER)
  • Handle vigilance activities including complaint intake and tracking
  • Participate in Post-Market Surveillance (PMS) data collection and analysis
  • Contribute to risk management documentation and updates
  • Perform clinical data evaluation and compliance checks
  • Coordinate with cross-functional teams (RA, QA, Clinical, Safety)
  • Ensure adherence to regulatory guidelines and SOPs

Qualifications & Eligibility

To apply for this clinical trial assistant job in Romsons, candidates must meet:

  • Education: M.Pharm / MSc (Life Sciences or related field)
  • Experience: 1โ€“4 years in clinical research / medical devices
  • Knowledge of:
    • PMCF & PMS processes
    • Clinical Evaluation (CER writing support)
    • Vigilance & complaint handling
    • Regulatory compliance (EU MDR preferred)
  • Strong documentation and analytical skills

Preferred Skills (High-Impact Keywords)

  • Clinical Trial Assistant (CTA)
  • PMCF (Post-Market Clinical Follow-up)
  • PMS (Post-Market Surveillance)
  • Clinical Evaluation Report (CER)
  • Medical Device Vigilance
  • Risk Management (ISO 14971)
  • Regulatory Affairs (Medical Devices)
  • Clinical Data Analysis

Benefits of This Role

  • Exposure to end-to-end medical device lifecycle
  • Hands-on experience in PMCF, PMS, CER & vigilance systems
  • Opportunity to work with cross-functional regulatory teams
  • Strong career pathway into:
    • Clinical Research Associate (CRA)
    • Regulatory Affairs Specialist
    • Medical Device Safety / Vigilance roles

Job Details

  • Company: Romsons Group of Industries
  • Role: Clinical Trial Assistant
  • Location: Noida, India
  • Experience: 1โ€“4 years
  • Employment Type: Full-time

Salary Insight (Estimated)

Based on industry standards for Clinical Trial Assistant jobs in Noida:

  • โ‚น3.5 LPA โ€“ โ‚น6.5 LPA (depending on experience and domain expertise)

How to Apply

Application Link

Clinical Trial Assistant Job in Romsons

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