Junior Manager*in (f/m/d) Clinical Operations

Do you want to help create the future of healthcare? Our name, Siemens Healthineers, was selected to honor our people who dedicate their energy and passion to this cause. It reflects their pioneering spirit combined with our long history of engineering in the ever-evolving healthcare industry.

We offer you a flexible and dynamic environment with opportunities to go beyond your comfort zone in order to grow personally and professionally. Sounds interesting?

Then come and join our global team as Junior Manager (f/m/d) Clinical Operations to help shape the future of Siemens Healthineers with your expertise in the healthcare industry.

Choose the best place for your work - Within the scope of this position, it is possible, in consultation with your manager, to work mobile (within Germany) up to an average volume of 60% of the respective working hours.

Your tasks and responsibilities:

• You support the planning, coordination, and operational implementation of clinical trials.
• You ensure adherence to clinical study protocols, SOPs, and regulatory requirements for clinical trials with medical devices.
• You work effectively in teams and with internal and external stakeholders in the areas of Clinical Affairs, data management, biostatistics, and contract generation.
• You assure standardized monitoring and site management.
• You monitor adherence to clinical trial budgets and schedules.

Your qualifications and experience:

• You have successfully completed your university studies in medicine, sciences, or health-related areas.
• You have several years of experience in the healthcare sector in the field of planning and conduction of international multicenter clinical trials in Europe and the US (additional geographies beneficial), preferably in the medical device industry or in Contract Research Organizations (CROs).
• You bring knowledge of relevant national / international standards and applicable rules and regulations for clinical trials, e.g., ICH-GCP, ISO 14155, 21 CRF (resp. parts), MDR and national implementations etc.
• You are experienced in the collaboration with study sites and service providers in the field of clinical research, e.g., CROs, Core Labs, as well as in the communication with ethics committees and competent authorities.
• You have experience in the development of CRFs and ideally with tools for data management and implementation of clinical trials (e.g., EDC, CTMS).

Your attributes and skills:

• You have fluent verbal and written communication skills in English and German.
• You are self-motivated to continuously develop your knowledge regarding clinical trials and clinical operations as well as relevant clinical disciplines and the Siemens Healthineers product portfolio.
• You have a strong ability to effectively communicate at all levels in an organization both internally and externally.
• You demonstrate flexibility and the ability to change priorities and adjust study activities and plans according to needs.

Our global team:

Siemens Healthineers is a leading global medical technology company. 73,000 dedicated colleagues in over 70 countries are driven to shape the future of healthcare. An estimated 5 million patients across the globe benefit every day from our innovative technologies and services in the areas of diagnostic and therapeutic imaging, laboratory diagnostics and molecular medicine, as well as digital health and enterprise services.

Our culture:

Our culture embraces different perspectives, open debate, and the will to challenge convention. Change is a constant aspect of our work. We aspire to lead the change in our industry rather than just react to it. That's why we invite you to take on new challenges, test your ideas, and celebrate success.

As an equal opportunity employer, we welcome applications from individuals with disabilities.