PHARMA BHARAT
PHARMACEUTICAL JOB PORTAL
No new notifications

Advertisement

Clinical Research Associate Job at Veeda Lifesciences

Published on

Veeda Lifesciences

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 documentationโ€”key skills for long-term growth in the pharma and CRO industry.

Advertisement

๐Ÿ“Œ 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

๐Ÿ”‘ Key Responsibilities

๐Ÿงช 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

๐Ÿ“„ 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

โš–๏ธ 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

๐ŸŽ“ 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

๐Ÿ’ผ Salary & Benefits

  • Estimated Salary: โ‚น3.5 LPA โ€“ โ‚น6.5 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

๐Ÿš€ 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:

  • 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.


๐Ÿ“ฅ How to Apply

Application Link

Share This Job

โœ… Job Details Copied!