08 Nov
|
Fortis
|
New Delhi
- Assist in the development and implementation of clinical trial protocols and study designs.
- Coordinate with cross-functional teams, including investigators, data managers, and statisticians.
- Conduct site feasibility assessments and coordinate site selection processes.
- Develop and maintain study timelines, budgets, and resource allocation plans.
- Ensure compliance with regulatory requirements and company policies.
- Collaborate with internal stakeholders to resolve issues and improve processes.
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
📌 Assistant Clinical Research (New Delhi)
🏢 Fortis
📍 New Delhi