The project manager position requires ability to execute complex clinical study operation activities as well as leading clinical design of multiple projects. The selected candidate will be responsible for delivery of these activities by execution, scheduling, budget, risk mitigation and resource management activities, when applicable.
The selected candidate must be proficient with IVD/device worldwide regulation (CE, FDA, ICH, etc.) and clinical study design. The candidate will perform technical review of clinical study design and documentation. Executes continuous improvement plan.
Clinical monitoring, people management, project management are must have.
The submitted candidates must have at least 3-5 years of experience in such a role.