Clinical Study Manager (f/m/x)

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 silence 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.

As a Clinical Study Manager (m/f/x), you will play a pivotal role in driving and executing the global clinical strategies defined within the Strategic Business Unit Microsurgery. You will oversee all clinical operations across various medical disciplines. Your responsibilities will include ensuring the progress of each while engaging with clinical sites in coordination with the medical affairs team and Contract Research Organizations (CROs).

lead the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and company standards

collaborative with cross-functional teams, including Strategic Marketing, Medical Affairs, R&D, and Regulatory Affairs, to align clinical strategies with business objectives

assist in the development of clinical marketing materials in coordination with the Marketing and Medical Affairs

provide training and support to clinical site staff to ensure adherence to study protocols and best practices

analyze and interpret clinical data, preparing reports and presentations for stakeholders

maintain strong relationships with clinical sites and key opinion leaders to foster collaboration and enhance study performance

master's degree (M.Sc.) in a relevant field; a Ph.D. in medical physics or an MD is preferred

minimum of two years of professional experience in a Clinical Research Organization (CRO) or a similar industry setting

additional experience in Clinical Affairs, Medical Affairs, or clinical applications within the medical device industry is a plus

excellent communication and presentation skills, with the ability to acquire complex information clearly

customer-oriented mindset with a proactive approach to relationship building and maintaining customer loyalty

proficient in English and German; proficiency in additional languages is advantage.

willingness to travel borders (up to 50%)