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Clinical Data Monitoring & eCRF Designer at MS Clinical Research.

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MS Clinical Research

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences, Biotechnology, Clinical Research

Bengaluru

1 - 5 Years

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Looking to build a career in clinical data management jobs in India? MS Clinical Research is hiring a Data Monitoring & eCRF Designer in Bengaluru. This is a strong opportunity for candidates interested in clinical research, eCRF design, and data monitoring roles, especially those aiming to work with real-world clinical trial data systems.

This role blends clinical data management, regulatory compliance, and eCRF development, making it ideal for candidates targeting entry-level to mid-level clinical research jobs in Bengaluru.

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Job Overview

  • Role: Data Monitoring & eCRF Designer
  • Company: MS Clinical Research
  • Location: Bengaluru, Karnataka, India
  • Job Type: Full-time, On-site
  • Experience: 1 – 5 Years
  • Industry: Clinical Research / Clinical Data Management

Key Responsibilities

Data Monitoring & eCRF Design

  • Design and develop electronic Case Report Forms (eCRFs) using Zoho Database aligned with study protocols
  • Perform clinical data monitoring to ensure data accuracy, completeness, and consistency
  • Conduct data validation, discrepancy management, and query resolution
  • Support User Acceptance Testing (UAT) and ensure system functionality
  • Troubleshoot eCRF issues and maintain smooth data flow across studies
  • Ensure compliance with GCP guidelines and regulatory requirements

Regulatory & Documentation Support

  • Assist in preparation and review of clinical trial documentation
  • Ensure consistency and compliance in clinical and regulatory records

Collaboration & Project Execution

  • Coordinate with clinical teams, investigators, and stakeholders
  • Manage multiple clinical studies simultaneously
  • Support database lock and clean dataset readiness for analysis

Required Qualifications

  • Bachelorโ€™s or Masterโ€™s degree in:
    • B.Pharm / M.Pharm
    • Life Sciences / Clinical Research / Biotechnology
  • Basic understanding of:
    • Clinical Data Management (CDM)
    • eCRF design and validation
    • ICH-GCP guidelines
  • Skills:
    • Strong analytical and problem-solving abilities
    • Attention to detail in clinical data review
    • Good communication and teamwork

Preferred Skills

  • Experience with Zoho Database or EDC systems
  • Knowledge of clinical trial processes and workflows
  • Familiarity with query management and data cleaning

Salary & Benefits

  • Estimated Salary: โ‚น3,00,000 โ€“ โ‚น6,00,000 per annum
  • Hands-on exposure to clinical trial data systems
  • Opportunity to work on real-world clinical research projects
  • Career growth in clinical data management and pharmacovigilance domains

How to Apply

Application Link

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