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• Conduct different types of monitoring visits (pre-study visits, site initiation visits, interim monitoring visits & close out visits)
• Develop and maintain site and investigator relationships to ensure clinical trials are managed efficiently

• Design and configure Master Batch Records within Rockwell PharmaSuite
• Translate manufacturing process requirements into compliant MES design solutions
• Ensure adherence to global templates, design principles, and regulatory requirements

• Engagement with the external regulatory environment within defined area of responsibility - Azerbaijan, Turkmenistan and Georgia
• Maintenance of registration and launch of new products in OTC and MD categories

• Development and integration of state-of-the-art machine learning algorithms for future ophthalmic and other medical devices
• Gain hands-on experience with multiple neural signal modalities

• Proven experience writing and editing documentation for an end-user audience
• Ability to quickly learn and understand complex procedures and concepts
• Ability to work with and understand functional engineering specifications for the software features/functions and the user interface

Design, implement, and maintain data pipelines that integrate multimodal, structured and unstructured clinical and surgical data from proprietary data collection systems and electronic health record systems, supporting both retrospective analyses and secure live or near-real-time data flows in...

Lead customer and product discovery end-to-end - from uncovering real problems to shaping valuable, usable, feasible, and viable solutions to the healthcare industry's most significant challenges...

• Develop and evaluate concepts for interactive guidance in navigated ENT surgery
• Design and implement proof-of-concept applications for surgical navigation systems
• Apply technologies such as computer vision, augmented reality, machine learning, and human-computer interaction