- 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 (India)
🏢 Advity Research
📍 India
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