Auditor
Veeda Lifesciences
Essential documents and study specific document review:.QA review of study specific documents like Protocol, ICF, patient diary, clinical study report etc.SOPs, GCP and applicable regulatory requirements.Essential documents review for clinical...
Last checked on April 30, 2026. We may earn a commission when you click through.
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Ahmedabad
📅 2026-04-12
About this role
Essential documents and study specific document review:.QA review of study specific documents like Protocol, ICF, patient diary, clinical study report etc.SOPs, GCP and applicable regulatory requirements.Essential documents review for clinical trials (including phase trials and patient based multisi
About the Company
Veeda Lifesciences specializes in providing comprehensive solutions in the clinical research and development sector.
Key Highlights
- ✓ Focus on quality assurance for clinical trials
- ✓ Review essential study documents like Protocol and ICF
- ✓ Ensure compliance with GCP and regulatory standards
- ✓ Opportunity to work in a pivotal role within healthcare
- ✓ Based in Ahmedabad, allowing for local industry engagement
💡 Honest Take: This job is crucial for maintaining standards in clinical trials, but expect a rigorous workload. It's a solid pick for those serious about quality in healthcare research.
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