- 6-month contract to start with the possibility of extension or conversion depending on performance and business needs
- Rate: $55-60
- Location: 100% Remote
- The Global Clinical Strategy Lead – Orthopedics & Robotics is responsible for developing and executing global clinical and health economic evidence strategies that support new product introductions, drive market adoption, maintain regulatory compliance, and strengthen market access initiatives across the product lifecycle. This role partners cross-functionally with R&D, Clinical Operations, Regulatory Affairs, HEOR, Medical Affairs, Marketing, and Commercial teams to ensure clinical evidence strategies are aligned with business objectives, regulatory requirements, and customer needs.
- The Lead identifies evidence gaps and develops comprehensive global evidence generation plans, including clinical study design, publication strategy, claims support, and real-world evidence initiatives. As a key contributor to new product development teams, this individual ensures the timely integration of clinical strategy into development programs, regulatory submissions, and commercialization pathways.
- In addition, the role collaborates externally with healthcare professionals, key opinion leaders, research institutions, and strategic partners to generate high-quality clinical evidence through company-sponsored studies, investigator-initiated research, and real-world data programs. This position plays a critical role in ensuring the Orthopedics and Robotics portfolio is supported by robust, scientifically sound evidence that drives clinical adoption, differentiates products in the marketplace, and supports long-term commercial success.
- Bachelor’s degree in Engineering, Design, Life Sciences, Clinical Sciences, or a related discipline required
- Prior experience within Orthopedics, Medical Devices, and/or Robotics required
- BS with 6+ years of relevant experience, MS with 3+ years of relevant experience, or PhD with 1+ year of relevant experience
- Strong understanding of clinical evidence generation, regulatory strategy, and product lifecycle management
- Experience collaborating across cross-functional and global teams in a matrixed environment
- Excellent communication, stakeholder management, and scientific presentation skills
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