Clinical Study Assistant (m/f/d)

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Your tasks:

• administrative tasks in the area of study coordination
• On-site or digital support for clinical trial centers as part of clinical trials of medical devices, in particular digital health applications (“medical app on prescription”) or an in vitro diagnostic device
• Monitoring and documentation of study inclusions and subsequent visits
• proactive communication with study doctors and study participants
• Provision of registration documents
• Communication with ethics committees and higher federal authorities
• Maintaining study databases and, if necessary, data entry
• Data retrieval and preparation for statistical evaluations
• Support with study documentation and presentation of results
• occasional assistance with administrative tasks
• Implementation of the legal requirements of MDR, MPDG and IVDR or of studies outside these regulations

Professional and personal qualification:

• Training as a medical documentary or study assistant (study nurse) or clinical research associate with experience outside the AMG
• Knowledge and experience in so-called decentralized digital studies or willingness to familiarise yourself with them
• very good MS Office skills (especially Excel)
• good understanding of medical issues and basic knowledge of scientific work
• very good written and spoken German and English skills
• strong communication skills, good language
• very high reliability and conscientiousness
• independent, very careful, structured and results-oriented action
• very good time and priority management as well as high organizational skills and a high level of service orientation, humor and authenticity
• reliable and situational presentation techniques for decision makers

Our offer:

• modern full-time workplace (40 h/w) in Berlin
• exciting tasks in a future-oriented industry with varied projects in the field of clinical research to implement regulations and laws for cutting-edge innovations
• committed college
• completely digitized studies
• established standard processes, quality management and innovative thinking
• structured and thorough training as well as continuing education and development opportunities
• Opportunity to take responsibility and implement your own ideas
• Benefits of a secure order situation due to satisfied regular customers and continuous office workload
• flat hierarchies, short decision-making processes in an established and long-standing team, and respectful supervisors who communicate on equal footing
• Self-image of work and leisure

We stand for equal opportunities. People with disabilities are recruited as a matter of priority if they are equally qualified. We would like to point out that the chosen job title also includes non-dual genders.