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Clinical Research Associate Job at Veeda Lifesciences

Published on

Clinical Research Associate

Veeda Lifesciences

Veeda Lifesciences logo

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences, Clinical Research, or related field

Ahmedabad, Gujarat, India

1 Year+

Verified Job

Online Application

Looking to build a career in clinical research jobs in India? A new opportunity has opened for a Clinical Research Associate (CRA) at Veeda Lifesciences in Ahmedabad, Gujarat. This role is ideal for candidates with a background in life sciences who want hands-on experience in clinical trial monitoring, GCP compliance, and site coordination.

With increasing demand for clinical research associate jobs in Ahmedabad, this position offers strong exposure to off-site monitoring, regulatory compliance, and clinical trial documentation—key skills for long-term growth in the pharma and CRO industry.


📌 Job Overview

  • Job Title: Clinical Research Associate
  • Company: Veeda Lifesciences
  • Location: Ahmedabad, Gujarat, India
  • Job Type: Full-Time
  • Work Mode: On-site
  • Experience Level: Entry to Mid-level
  • Industry: Clinical Research / CRO

🔑 Key Responsibilities

🧪 Off-Site Monitoring

  • Conduct initial site visits and train site personnel as per study protocols
  • Perform routine monitoring visits during different study phases
  • Ensure site readiness and compliance with protocol requirements

📄 Communication & Documentation

  • Handle feasibility assessment questionnaires and site coordination
  • Prepare essential reports:
    • Pre-Study Qualification Reports
    • Site Initiation Visit Reports
    • Monitoring Visit Reports
    • Close-Out Visit Reports
  • Collect and manage study documents such as:
    • Calibration reports
    • Agreements
    • Regulatory documents
  • Provide study tools like logs, recruitment trackers, and data templates

⚖️ Audits & Compliance

  • Ensure compliance with GCP guidelines, SOPs, and regulatory requirements
  • Train site teams on protocol and regulatory updates
  • Respond to QA/QC audits and sponsor/regulatory queries
  • Support root cause analysis and corrective actions

🎓 Qualifications & Skills

  • Education: B.Pharm, M.Pharm, Pharm.D, BSc/MSc Life Sciences or related field
  • Strong understanding of:
    • Clinical trials & monitoring
    • Good Clinical Practice (GCP)
    • Regulatory guidelines
  • Good communication and documentation skills
  • Ability to manage multiple sites and timelines

💼 Salary & Benefits

  • Estimated Salary: ₹3.5 LPA – ₹6.5 LPA (based on experience)
  • Opportunity to work with a leading CRO in India
  • Exposure to global clinical trials
  • Skill development in clinical operations & regulatory compliance
  • Career growth in clinical research associate roles

🚀 Why This Role Matters

The demand for clinical research associate jobs for freshers and experienced professionals is growing rapidly in India. This role at Veeda Lifesciences offers real-world exposure to:

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  • Clinical trial lifecycle
  • Site monitoring and management
  • Regulatory inspections and audits

If you’re aiming for a long-term career in clinical research, pharmacovigilance, or regulatory affairs, this is a strong entry point.


📥 How to Apply

Application Link

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