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A leading company in the dental medical device sector is seeking a Regulatory Medical Writer to join their Real-World Evidence Team in Madrid. The successful candidate will be responsible for authoring PMCF Plans and Reports, ensuring compliance with EU regulations, and collaborating with various stakeholders to deliver key documentation. This full-time position offers an opportunity to contribute significantly to the maintenance of a comprehensive portfolio in the European market.
Regulatory Medical Writer
As a regulatory medical writer, you will play a crucial role in our Real-World Evidence Team, authoring Post Market Clinical Follow-Up (PMCF) Plans and Reports, contributing to the Clinical Evaluation, and Post-Market Surveillance documentation. In this role you will collaborate with internal and external partners to evaluate clinical data from diverse sources. By leveraging your regulatory writing skills and experience, you will directly contribute to fulfilling our post-market clinical data obligations under the Medical Device Regulation, leading to a successful maintenance of our comprehensive dental medical device portfolio on the European market.
The position is a 100% position (40hrs/week) as Regulatory Medical Writer for Post-Market Clinical Follow-Up. Your workplace will be Straumann group’s Southern European Hub located in Madrid, Spain but you will be working directly with the Real-World Evidence Team at Straumann’s Headquarters in Basel, Switzerland.
Your responsibilities:
Your experience / personal profile:
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or disability.
Employment Type:Full Time
Alternative Locations:Spain : Madrid
TravelPercentage:0 - 10%
Requisition ID: 18104