Clinical Operations Manager
il y a 1 jour
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 180,000 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._
- Our Instruments division is the world leader in development and deployment of modern solutions with high technological value to our customers Opticians and Optometrists, in the cutting/mounting of correction lenses and in refraction and diagnosis of eye diseases. Our mission is to provide vision professionals with equipment and services that are perfect responses to their business needs and help them build a strong and trusting relationship with their patients. _
- Product innovation driven by our R&D teams, the global development of our distribution networks and the strong integration of our business with the other entities of the Essilor Luxottica Group are the main drivers of the strong growth that the Instruments Division has been experiencing for 5 years._
Within the Essilor Instruments department, the Clinical Operations Manager will join the Scientific Department and will be responsible for coordinating all clinical activities, managing clinical operation portfolio and budget.
You will draw up, implement and coordinate the development plan for studies on the Optometry products range for which you are responsible, ensuring compliance with regulations and deadlines with international regulations.
You will be involved in the following activities:
- Organizing clinical investigations and usability tests as part of projects covered by regulations relating to the development of medical products.
- Redaction of scientific documents required for the registration of medical products (Clinical Evaluation) and their monitoring (Post Market Clinical Folow up) on the market in support of regulatory compliance.
- Carry out scientific and medical monitoring as well as literature reviews.
You will ideally have some of the skills and experience below:
- Educational Background in **Master Vision Science (BAC +5) or Clinical Developement**:
- At least **5- 10 years experience in Clinical Studies (optics/medical devices)**:
- Strong problem solving skills
- Very good knowledge of clinical trial procedures and good clinical practice
- Ability to interpret and use scientific information in summary form
- Ability to manage projects in a highly constrained environment
- Ability to prioritise objectives and manage their achievement
- Lead, supervise and motivate a team
- Work collaboratively and liaise with other teams within the company (Scientists, Regulatory Affairs, Quality R&D etc), in line with company strategy, to drive projects forward.
- Due to the international scope of the role, you are able to communicate in both English and French.
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