Skills:
Medical Device R&D, protocol deviations, Clinical Trials, Biomedical Engineer,

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