Job Description
In this role, you will be responsible for executing the clinical evidence strategy for medical devices, and support the development of this strategy, to enable new and continued global market access. Partner with cross-functional teams (e.g., Marketing, R&D/NPD) to develop short- and long-term clinical evidence strategies, providing scientific expertise to guide business decisions. Develop and execute clinical regulatory strategies to support global market access, including authoring clinical sections of regulatory submissions and evaluations. Lead all aspects of clinical research: study design, execution, reporting, budgeting, contracting, monitoring, and ensuring compliance with Good Clinical Practice (GCP). Support the development and maintenance of procedures and systems to ensure effective management of clinical studies and evaluations in compliance with global regulations. Generate clinical data aligned with business strategy through pre- and post-market trials, efficacy studies, registries, surveys, and literature reviews.
About Stryker
Stryker is one of the world’s leading medical technology companies and, together with its customers, is driven to make healthcare better.