Clinical Research Director
As a Clinical Research Director, you will be responsible for overseeing the planning, execution, and completion of clinical studies in accordance with regulatory guidelines. This involves coordination and management of multicenter applications with authorities and ethics committees, including document preparation and administration for pre- and post-market studies.
You will also contribute to scientific publications and publication strategy, including storyline development, and prepare and manage safety reports as part of your key tasks.
Key Responsibilities:
* Lead project teams for process optimization, documentation improvement, and data preparation
* Manage multicenter applications with authorities and ethics committees
* Coordinate document preparation and administration for pre- and post-market studies
* Contribute to scientific publications and publication strategy
* Prepare and manage safety reports
Requirements:
* Masters' degree or higher in Life Sciences
* At least 2 years of professional experience as a Clinical Research Manager, ideally in the field of medical devices
* Good knowledge of regulatory requirements in medical technology
* Experience with MS Office, review tools, reference management, and document management is an advantage
* Very good command of English, both written and spoken; basic knowledge of German is required
What We Offer:
* Central location
* Employee discounts
* Flexible hours
* International environment
* Onboarding
* Workplace well-being