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At Fresenius Medical Care, we are the global leader in kidney care, committed to improving the lives of patients with chronic kidney disease. Our mission is to deliver high-quality, innovative products, services, and care across the entire healthcare journey. Guided by our vision—"Creating a future worth living. For patients. Worldwide. Every day."—we work with purpose and compassion, supported by a global team of over 125,000 employees. Our values guide how we work: We Care for our patients, each other, and our communities. We Connect across teams and borders to deliver excellence together. We Commit to doing things the right way— growing with purpose and leading kidney care with integrity and innovation.
Job Responsibility:
Selection of competent and appropriate clinical research organisation (CRO) and other service providers
Negotiation of legal and financial terms and conditions concerning agreement with CRO or other service provider for preparatory activities and performance of planned studies
Continuous exchange with CRO and other qualified service providers in regular meetings ("Jour-fixe")
Collaboration with FMC concerning concept, planning and performance of planned studies
Collaboration with FMC concerning preparation and review of synopsis´ and study protocols of planned studies
Preparation of concept, planning and performance of meetings of the (coordinating) investigators of the ongoing studies
Communication with all involved (coordinating) investigators of the studies, e.g., concerning the implementation of the study in the specific countries or for review of study documents etc.
Training of field sales force amongst others of participating countries taking part in the planned studies
Provision of regular updates concerning the ongoing studies within FMC core team
General collaboration with other departments of Fresenius Medical Care concerning studies (e.g., compliance and legal department etc.)
Compliance qualification and contracting of study sites (OnBoard process) on behalf of Fresenius Medical Care
Requirements:
Scientists or medical professionals with experience in conducting clinical trials of drugs and medical devices
Knowledge and experience in planning and conducting clinical trials, regulatory requirements for clinical trials, and the further utilization of clinical data (clinical evaluation, scientific publications, presentations)
Experience in project management
Structured, goal-oriented approach to work
Interest in new tasks
Analytical skills
Collaborative personality
Ability to mediate between unclear or conflicting positions
Ability to handle stress
Confident demeanor
Strong ability to concentrate
Ability to prioritize
Accuracy and reliability
Good self-organization
Team player and strong communication skills
Excellent English language skills (spoken and written)
Knowledge of pulmonology and cardiology
Knowledge of nephrology/dialysis as well as other clinical conditions and treatment methods
Experience in scientific research and working with scientific literature
What we offer:
Individual opportunities for self-determined career planning and professional development
A corporate culture in which there is enough room for innovative thinking - to find the best solution together, not the quickest one
A large number of committed people with a wide range of skills, talents and experience
The benefits of a successful global corporation with the collegial culture of a medium-sized company