• Develop and execute subcontract strategies to align with program and organizational objectives • Lead negotiations to establish subcontract agreements with favorable terms and conditions • Monitor and evaluate subcontractor performance using defined metrics • Collaborate with cross-functional teams, such as engineering, finance, and program management • Identify potential risks associated with subcontracting activities and develop mitigation strategies • 25% Travel to supplier site locations

• Assists sales representatives with surgeon trainings, hospitals robotic development, and overall territory management • Guides technical in-services for customers to include OR staff, surgeons, etc. • Sells benefits of advanced technology to existing robotic users to contribute to team overall quotas • Gains experience in goal setting, mapping, and attaining in preparation for quota bearing role to follow CTA position • Manages administrative tasks: reporting of sales/procedures, outcomes of sales activities, submission of expense reports

• Works closely with the Director of Procurement to help support the procurement department. • Distributes and executes NDCA’s for new suppliers. • Viewpoint data entry support. • Participates in Project conference calls and supplier meetings. • Distributes RFQ’s to suppliers and tracks progress. • Draft’s Purchase Orders for Major Equipment. • Draft’s Change Orders for Major Equipment and Subcontractors. • Tracks and supports all aspects of the procurement process after order execution.

• Preparing, compiling, and submitting regulatory and ethics documentation, including clinical trial applications and ethics committee submissions • Coordinating with internal teams, sponsors, regulatory authorities, and investigative sites to secure required approvals and authorisations for study initiation • Maintaining accurate and inspection-ready records of regulatory submissions, approvals, and essential study documents • Supporting study teams in the development, review, and management of key study documentation, including protocols, informed consent forms, and investigator brochures • Participating in study start-up meetings, providing guidance on regulatory requirements, timelines, and activation strategies • Tracking study start-up milestones and proactively identifying and resolving issues that may impact activation timelines • Ensuring all activities are conducted in accordance with applicable regulations, ICH-GCP guidelines, and company SOPs