WHO WE ARE
We are EssilorLuxottica, a global leader in the design, manufacture and distribution of ophthalmic lenses, frames and sunglasses. The Company brings together the complementary expertise of two industry pioneers, one in advanced lens technologies and the other in the craftsmanship of iconic eyewear, to create a vertically integrated business that is uniquely positioned to address the world’s evolving vision needs and the global demand of a growing eyewear industry.
With over 200,000 dedicated employees in 150 countries driving our iconic brands, our people are creative, entrepreneurial and celebrated for their unique perspectives and individuality. Committed to vision, we enable people to “see more and be more” thanks to our innovative designs and lens technologies, exceptional quality and cutting-edge processing methods. Every day we impact the lives of millions by changing the way people see the world.
JOB SCOPE AND MAIN RESPONSIBILITIES:
The Clinical Project Manager/ Senior Manager oversees the planning, execution and completion of clinical trials led by the department WW, by ensuring compliance with applicable laws, standards and regulations. The main deliverables are the Clinical Evaluation Report, clinical evidence supporting product claims and medical writings. This is a cross-departmental function, with strong collaborations with global R&D teams, Medical & Professional Affairs and Regulatory Affairs.
AREAS OF RESPONSIBILITIES AND RELATED ACTIVITIES:
- Leading the Clinical Strategy discussions and proposing relevant clinical trials plan
- Designing, organizing and managing clinical trials worldwide
- Acting as the global R&D referent in clinical trials design by providing guidance and support to the clinical operation teams WW
- Supporting the medical device claims development by providing strong clinical evidence, in close collaboration with R&D, Medical & Professional Affairs, and Regulatory Affairs teams
- Participating in the medical writings with upstream research department and Medical & Professional Affairs
NETWORK OF INTERACTION:
INTERNAL : R&D, Medical & Professional Affairs, Regulatory Affairs, Marketing
EXTERNAL : Clinical Research Organizations, Hospitals, Clinics, Universities, Researchers
TECHNICAL SKILLS - PORTRAIT OF A PERFECT CANDIDATE
- Educational Background in Ophthalmology/Vision Sciences/Medical Sciences/Pharmacology
- At least 10 years of experience in Clinical Research, in Medical Devices industry is a plus
- Strategic thinking, leadership insight, and a deep understanding of regulatory landscapes.
- Solid experience with managing clinical trials from initial phase to post market surveillance.
- Solid experience in developing Clinical Strategy development.
- Scientific publications.
- Biostatistical analysis.
- Strong problem-solving skills.
