04 Sep
|
Fortis
|
New Delhi
- Assist in the development and implementation of clinical trial protocols and study designs.
- Coordinate with cross-functional teams, including data management, biostatistics, and medical writing.
- Conduct literature reviews and analyze data to identify trends and areas for improvement.
- Develop and maintain databases for tracking clinical trial progress and patient information.
- Collaborate with investigators and site staff to ensure compliance with study protocols.
- Prepare and review study-related documents, such as informed consent forms and case report forms.
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📌 Assistant Clinical Research (New Delhi)
🏢 Fortis
📍 New Delhi