At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging. **What You Can Expect** This global leadership role is responsible for clinical evidence strategy and execution of studies to ensure the scientific validity, regulatory compliance, and overall effectiveness of clinical research and outcomes related to Zimmer Biomet’s full line of products. The role collaborates with other departments to ensure the successful research to support real-world application. The incumbent will also develop and execute the direction and plans for global strategies that inform and support patient access, reimbursement and the value positions of Zimmer Biomet’s products and ecosystem of solutions. Additionally, this role will develop a robust data publication strategy to support commercialization efforts and create shareholder value. **How You'll Create Impact** + Ensure the right talent in the right roles to drive the right strategy and culture for creating a worldclass Clinical Affairs organization + Act as a consultant to senior management on product marketing strategies in relation to evidence-based practice and value proposition + Direct the development and execution of comprehensive Clinical evidence programs and budgets to meet company sales and profit objectives and optimize global market opportunities + Use scientific knowledge in evaluating clinical and non-clinical evidence of product safety and efficacy for marketed devices, new products and potential new product acquisitions + Oversee the management of clinical trial data, including data collection, cleaning, analysis, and reporting + Ensure clinical trials are rigorously designed and conducted to generate reliable and relevant evidence + Lead the development, management, and communication of clinical evidence strategy and plan to facilitate market access, reimbursement, messaging for all ZB business units + Develop a proactive, robust coordinated and targeted publication strategy to address and monetize key areas of company focus + Ensure regular cadence of publications, including but not limited to peer-reviewed publications and podium presentations **What Makes You Stand Out** + Boldo Articulates a compelling and inspiring visiono Challenges the status quoo Takes calculated riskso Cultivates new ideas and inspires and motivates others to do the same + Insightful and Innovativeo Has an entrepreneurial mind set, leveraging data, insights, and experience to bring strategy to lifeo Seeks new and innovative solutions o Brings a global perspective to the organizationo Future focused o Simplifies the complex + Collaborativeo Creates a sense of shared purpose by demonstrating commitment to ZB’s mission, vision, and cultureo Takes an inclusive approach to ensure diverse points of view are consideredo Empowers others to do their jobs well and proactively offers coaching o Builds strong relationships across regions, functions, internal and external stakeholders with a spike in customer centricity + Proactiveo Commitment to achieve results with a sense of urgency, even in the face of challenges, inspiring the same mindset within the team.o Anticipate setbacks and problems and proactively develops solutionso Drives a culture of accountability and sets high standards for self and otherso Takes decisive action using facts and data to drive decision-making + Agileo Identifies and embraces opportunities to learn and grow, evolving and adapting approach to drive collaboration and resultso Flexible approach: self modulates based on audience; embraces changes and proactively seeks approaches for transforming organizationso Demonstrates self-awareness and ability to self-regulate and manage emotions under times of significant stresso Learns from mistakes and pivots to alternative options **Your Background** + Ability to bring structure, process, and operating mechanisms to foster prioritization of key opportunities and methodology to the strategy and approach + Understanding of med-tech industry and device markets + Creates new ideas and processes, encourages others to try new approaches and takes risks. Enhances performance through unique and leading-edge actions and technologies + Demonstrates principled leadership and sound business ethics; shows consistency among principles, values and behaviors + Knowledge of regulatory requirements relating to clinical investigations and product approvals + Extensive knowledge of medical device, clinical study design, protocol development, and statistical analysis + Knowledge of the clinical research process and methodology as well as healthcare economics and reimbursement + External insights gleaned from diverse experiences + Comfortable working in a matrix environment **Compensation:** Expected Compensation: $300,000-$380,000. Plus bonus/LTI. EOE