Coordinate and manage clinical trials, ensuring compliance with regulatory requirements and company standards.
Develop and implement effective clinical trial management systems to enhance efficiency and productivity.
Collaborate with cross-functional teams, including medical specialists, researchers, and administrative staff, to achieve project goals.
Conduct site visits to monitor clinical trials, identify issues, and provide guidance to investigators.
Analyze data from clinical trials to identify trends, risks, and areas for improvement, and develop reports to communicate findings to stakeholders.
Ensure accurate and timely documentation of clinical trial activities, including protocols, case report forms, and investigational reports.

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📌 Clinical Secretary Gurugram
🏢 mCura Mobile Health
📍 Gurugram