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 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**:
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 evaluate clinical evidence requirements on specific products/brands and gather required clinical data in a cost effective, timely, and efficient fashion. Individual will work closely with Clinical Strategy to ensure projects are aligned with business needs.

**How You'll Create Impact**:

- Critically reviews and analyzes pertinent internal and external scientific content - Evaluate documents and reports that provide scientific or economic rationale for the use of marketed Zimmer Biomet products, including those created by AI for accuracy and appropriateness.
- Participate in PMS process as the clinical representative. 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.
- Strategically partners with Clinical Affairs & Brand Marketing teams to collaborate, understand, and proactively review marketing deliverables as well as scientific publications and presentations.
- Support development of clinical data summary by Clinical Evidence to meet tender/reimbursement requirements.
- Proactively drive clinical research outcomes by developing publication strategies and plans.
- Collate available clinical evidence for key products and assist in delivering effective presentations on Zimmer Biomet products for multiple audiences.
- Creates and maintains a database of published literature with summaries of key findings for assigned product lines.
- Grows and maintains collaborative working relationships with internal partners to provide scientific and marketing content development support.
- Reviews and updates scientific communication dashboards as requested.
- Supports the development of regulatory documents or reviews based on company needs including regulatory inquiries.
- Represents Scientific Communications within Clinical Marketing and other cross-functional teams as needed.
- Creation and maintenance of a claims matrix.
- 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
- Ability to assist and mentor other team members
- Proficient in Microsoft Office Suite
- Good Clinical Practice guidelines

**Your Background**:

- Bachelor’s Degree required; concentration in Health, Life Sciences, or Engineering preferred
- Post-graduate degree preferred
- Minimum of three (3) years of experience in clinical research, regulatory, or medical writing environments for medical devices, or an equivalent combination of additional education and experience
- Experience in orthopedic medical device marketing and regulations preferred.

**Travel Expectations**:
Up to 10%

EOE/M/F/Vet/Disability