Responsibilities include conducting protocol-specific tasks, managing clinical operations. The role will also involve planning and overseeing the life cycle of clinical trial supplies while ensuring compliance with regulatory requirements and operational efficiency. Collaborative interaction with teams to streamline the execution of clinical research projects is a key aspect of the role.

Qualifications

• Experience with Protocol development and implementation.
• Knowledge and expertise as a Clinical Research Associate and in managing Clinical Research activities.
• Proficiency in Clinical Trials design, monitoring, and management.
• Understanding of Research methodologies and analysis in the clinical domain.
• Strong skills and experience in Clinical Operations, including planning and execution.
• Excellent organizational, communication, and analytical skills.