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0.0 - 1.0 years
2.0 - 5.0 Lacs P.A.
Hyderabad/Secunderabad, Pune, Bengaluru
Posted:3 days ago| Platform: 
Work from Office
Full Time
Should have knowledge in clinical research studies Monitoring of Clinical studies conducted at various CROs located globally as per ICH/GCP, applicable regulatory requirements, protocols and SOPs. Perform Site visits (i.e. Site Selection Visit) Required Candidate profile Strong understanding of clinical trial processes and regulatory requirements. Excellent clinical assessment skills and a commitment to patient safety and ethical research practices.
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