What You Will Be Doing Responsible for taking leadership to meet, collaborate and initiate clinical trials at various healthcare facilities. Prepare documentation for seeking permission to initiate clinical trials. Responsible for managing the healthcare facilities' requirements, needs, and help needed. Delivers results that have a direct impact on the successful completion of the clinical program. Coordinates with PM and communicates to them progress and critical issues that may impair trial progress. Train and guide site staff in the protocol and trial procedures to minimize protocol deviations (PDs). Train site staff in safety information handling devices and systems. Monitor & review the process and maintain the database in an organized system. Identify potential risks/difficulties and proactively take action to prevent or mitigate them. Ensure collaboration with and deliverables from. Collection and management of essential documents Team involvement and participation in meetings. Preferred Qualifications Biomedical Engineer bachelor's degree Core Competencies Project Management skill set Problem-solving Decision making Delegation skills Relationship Management and influencing skills Oral and written communication Time management Business English Organizational and planning skills Ability to work effectively in a team/matrix environment on multiple projects Proven ability to work independently and effectively handle multiple priorities in a fast-paced environment Demonstrable Risk Management skills Delivery and risk-focused Adaptability and Flexibility
