Company Description

For 80 years, Anthogyr has been designing, manufacturing, and distributing medical devices that enable dental health professionals to treat millions of patients worldwide.
Based in the heart of the Alps, Anthogyr is a human-sized company that has become a key player in dental implantology in France and in other fast-growing markets such as China.
Since 2019, Anthogyr has been part of the Straumann Group, the global market leader, strengthening its presence in key international markets. Within this global organization, we offer you the opportunity to grow in a supportive and stimulating professional environment, as part of a dynamic team and in an attractive living setting.

Introduction

As a Project Manager in Clinical Studies and Scientific Communication, you will play a key role in connecting clinical research with meaningful, evidence-based communication. Positioned within the Research and Clinical Affairs function, you will contribute to the development of scientific content that supports both medical education and business objectives.
Based in Sallanches, you will collaborate with cross-functional teams and external partners to ensure that clinical insights are translated into clear, impactful communication. This role offers the opportunity to work at the intersection of science, education, and innovation within a global healthcare environment.

Your Role

In this role, you will:

• Develop and implement a scientific communication plan aligned with business and clinical objectives
• Translate clinical data into clear, evidence-based content for medical education and communication channels
• Collaborate with product users and external partners to co-create and maintain up-to-date scientific materials
• Support and participate in medical education initiatives, ensuring accurate and accessible communication of scientific information
• Contribute to the setup, coordination, and monitoring of clinical studies in collaboration with internal teams
• Apply innovative approaches to maximize the value and visibility of clinical data

Your Profile

Must-have:

• Advanced degree in a relevant health or life sciences field (e.g., Master's, PharmD, PhD or equivalent)
• Experience in scientific communication and/or medical education
• Strong medical writing skills and ability to communicate complex information clearly
• Knowledge of Good Clinical Practice (GCP) and medical device regulatory standards
• Project management capabilities with the ability to manage multiple priorities
• Proficiency in English and French (written and spoken)

Nice-to-have:

• Experience in implantology or a related medical device field
• Familiarity with digital communication platforms and AI-supported tools

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or disability