0 - 1 years
2 - 5 Lacs
Posted:3 weeks 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.
Gratisol Labs
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My Connections Gratisol Labs
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Experience: Not specified
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