The MUL – CT combines research, teaching, and patient care in an innovative framework and offers diverse career opportunities, first-class continuing education programs, and a state-of-the-art working environment in the heart of Cottbus. 

We are looking for you as

Coordinator (m/f/d) for clinical trials

at the earliest possible date.

Shape the future of medicine with us! 

Your area of ​​responsibility

• Administrative study preparation: Preparation and submission of documents to ethics committees and authorities, planning of study initiations
• Coordination and communication: Support in the planning and execution of study-related meetings, interface between investigators, sponsor, study personnel and external partners.
• Study logistics & documentation:  Maintenance of study-related documents and data, support with data management
• Quality & Compliance:  Ensuring compliance with GCP, regulatory requirements and internal processes, preparation for audits and inspections
• Training & Support:  Organization of training courses for study staff, support of the team in study-specific processes.

Your profile

• Qualification: Completed studies or training in the medical, scientific or health-related field
• Industry experience:  Ideally, experience in the medical or healthcare sector; relevant professional experience and knowledge of GCP are advantageous.
• IT skills:  Proficient use of MS Office
• Language skills:  Very good German skills (min. level C1) and good English skills
• Soft skills:  High reliability, loyalty and commitment, structured and independent work style, excellent communication skills and strong organizational talent
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