Published: 29 April 2024
Ballaigues
100%
Unlimited employment
Dentsply Sirona
The Clinical Compliance Manager is responsible for the following scope:
The responsibilities start during the product development process and apply for the Dentsply Sirona medical device portfolio – with focus on endodontic products – throughout each product’s entire life cycle. When performing Clinical Evaluations and PMCF the Clinical Compliance Manager follows the applicable laws, guidelines, and internal processes.
The responsibilities of the Clinical Compliance Manager also include the management of consultants as well as the input / support for strategic planning of the document preparation.
Role and Responsabilities:
Clinical Evaluations
Post-Market Clinical Follow-up (PMCF)
Miscellaneous
Requirements and Qualification:
You hold at least a Master’s Degree in Life Sciences, Bioengineering, dentistry or a related subject. A PhD or doctoral degree would be a plus. You have a profound knowledge and a minimum of 4+ years working experience in the field of Clinical Evaluations, Medical Writing or Clinical Research within the medical device sector, preferably related to dental medical devices and/or dental health.
At Dentsply Sirona we offer a market conform salary, very attractive benefits, and an informal working environment. We are a diverse workforce and are passionate about the work we do!