Preferred Skills:
Experience in Monitoring Clinical Trials across phases (I-IV).
Knowledge of Regulations and Guidelines.
Experience in conducting site feasibility assessments and managing site qualification processes.
Experience with therapeutic areas such as Oncology and Neurology is a plus.
Detailed Responsibilities:
Manages and monitors the progress of clinical trials across multiple sites, ensuring compliance with study protocols, regulatory requirements, internal SOPs and quality assurance processes.
📌 Cra Hyderabad
🏢 Advity Research
📍 Hyderabad
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