Senior Specialist, Clinical Strategy

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 talent 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 included, respected, empowered, and recognized. What You Can Expect The Senior Specialist, Clinical Strategy serves as a key partner in shaping and advancing clinical strategy across assigned digital and enabling technology platforms globally. This role leads execution of clinical strategy activities, including support for new product introduction, evidence planning, claims support, and publication strategy input. As a key cross-functional partner, this individual works closely with Business Unit, Regulatory Affairs, and R&D teams to help translate clinical strategy into actionable plans and execution across the broader Clinical Affairs organization. How You'll Create Impact Lead execution of clinical strategy activities for assigned products, platforms, or therapy areas Contribute to development and maintenance of clinical evidence plans across the product lifecycle, including new product support and post-market needs Partner with cross-functional stakeholders to align clinical activities with business, regulatory, and development priorities Provide clinical input to support evidence needs related to product claims, regulatory submissions, scientific communications, and other business needs Support development of clinical content, evidence summaries, and strategic recommendations for internal stakeholders Contribute to publication and dissemination planning in alignment with broader clinical and business objectives Serve as a clinical point of contact for assigned initiatives, studies, or external research partners, as needed Help promote consistent execution of clinical strategy across internal teams and stakeholders Provide guidance and informal mentorship to less experienced team members, as appropriate What Makes You Stand Out Ability to work independently and manage complex projects within defined scope Strong cross-functional collaboration and communication skills Ability to translate clinical and scientific information into clear, practical recommendations Sound judgment in balancing clinical, regulatory, and business considerations Strong organization, prioritization, and follow-through Ability to influence stakeholders without direct authority Education and Experience Bachelor's Degree and 4 years of relevant experience, or Associate's Degree and 6 years of relevant experience, or High School Diploma or Equivalent and 8 years of relevant experience Bachelor’s degree in life sciences, health sciences, clinical research, public health, engineering, or a related field and relevant professional experience in clinical, scientific, regulatory, or product support roles is strongly preferred Background in medical devices, digital health, healthcare technology, or other regulated healthcare environments preferred Experience working with cross-functional stakeholders such as Regulatory Affairs, R&D, product teams, and commercial partners preferred Familiarity with clinical evidence planning, study support, scientific communications, or publication support preferred Travel Expectations Up to 15% EOE/M/F/Vet/Disability Expected Compensation: $110,500 to 125k, plus target bonus