Clinical Strategy Lead

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 position will serve as the Clinical Affairs business partner and interface with other functional areas and Team Members including but not limited to: assigned business units (BU), clinical operations, development, quality, global/regional marketing, regulatory affairs, PMS teams, medical writers, market access and the BCDM team. The Clinical Strategy Lead will enforce clinical evidence requirements on specific products/brands and gather required clinical data in a cost effective, timely, and efficient fashion, and work closely with Clinical Operations to ensure projects are aligned with evidence needs to support business needs.

How You'll Create Impact

• Implements proactive clinical evidence plans on products/brands based on Marketing/BU claims, regional needs, Market Access, Post Market Surveillance (PMS), and Regulatory Affairs needs.
• Participates in PMS process as the clinical team member. May provide literature searches, registry data or study results for annual reports, notified bodies or other internal and external needs. Oversight of PMS commitments and aligning study outputs to PMS reviews.
• Creates Project Needs Documents for newly identified clinical research projects, including Health Care Provider (HCP) nominations and Maximum FMV analyses for Investigator Initiated Research studies.
• Supports development of clinical data summary by Clinical Evidence to meet tender/reimbursement requirements.
• Drives proactively clinical research outcomes by developing publication strategies and plans.
• Collates available clinical evidence for key products, and assists in delivering effective presentations on Zimmer Biomet products for multiple audiences.
• Serves as a research services manager for select sites in conjunction with the External Research Process.
  
  

This is not an exhaustive list of duties or functions and might not necessarily comprise all of the essential functions for purposes of the Americans with Disabilities Act.

What Makes You Stand Out

• Sets priorities consistent with company goals and focuses on high priority opportunities
• Allocates resources (e.g. time, dollars) consistent with priorities
• Outstanding organizational skills and attention to detail
• Strong communication skills across all levels of the organization
• Strong knowledge of applicable regulations governing clinical studies
• Proficient in Microsoft Office Suite
• Good Clinical Practice guidelines
  
  

Your Background

• Bachelor’s Degree required; concentration in Health, Life Sciences, or Engineering preferred
• Minimum of five (5) years of experience in a clinical research environment, or an equivalent combination of additional education and experience
  
  

Travel Expectations

Up to 20%

Compensation

Salary Range: $100,000 - $107,500 USD

EOE/M/F/Vet/Disability

3159