Jobbeschreibung
Step out of your comfort zone, excel and redefine the limits of what is possible. That's just what our employees are doing every single day – in order to set the pace through our innovations and enable outstanding achievements. After all, behind every successful company are many great fascinating people.
In a spacious modern setting full of opportunities for further development, ZEISS employees work in a place where expert knowledge and team spirit reign supreme. All of this is supported by a special ownership structure and the long-term goal of the Carl Zeiss Foundation: to bring science and society into the future together.
Join us today. Inspire people tomorrow.
Diversity is a part of ZEISS. We look forward to receiving your application regardless of gender, nationality, ethnic and social origin, religion, philosophy of life, disability, age, sexual orientation or identity.
Apply now! It takes less than 10 minutes.
Seeing beyond - future of medical technology
For more than 100 years, ZEISS medical technology has been driving progress in ophthalmology and microsurgery. In ophthalmology, our solutions help to maintain and improve people's vision at every stage of their lives. In microsurgery, our solutions enable targeted interventions on diseased tissue so that small and sensitive organs continue to function optimally. Medical technology from ZEISS supports medical professionals in improving the lives of patients worldwide. The fact that our actions have a direct impact on people's well-being is what drives us every day.
Your role
Supporting Clinical Study Project Managers in planning and conducting clinical studies with medical devices (primarily Intraocular Lenses) according to applicable regulations and guidelines:
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Engagement in the formulation of study documents (e.g. test plans, monitoring documents, Case Report Forms/CRFs),
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Maintain, keep track of, and file study documentation (e.g. budget monitoring, Trial Master Files/TMFs)
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Prepare data evaluations
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Coordinate the storage and logistics of examination devices applied in the clinical studies.
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Request quotes from external service providers and prepare comparisons, coordinate the signing process and maintain contracts.
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Carry out literature searches and manage the literature database
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College or university qualification (e.g. bachelor's), preferably in optometry/ophthalmology, medicine, medical technology, or natural sciences.
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Relevant professional experience, preferably in clinical affairs/clinical operations within the medical device/pharma sector or with CROs.
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Dedication and innovative spirit along with excellent communication and organizational abilities in a global setting
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Very strong MS Office skills (e.g., Excel)
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A work style that is self-sufficient, team-focused, and highly committed
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Confident oral and written communication in German and English
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Quick comprehension, high level of care, motivation and initiative