Assistant Clinical Research

• 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.

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