Study Coordinator at the Center for Oncology – Clinic for Radiation Therapy and Radiooncology

Collection of data and reference findings and support of physicians in planning possible study participation Submission and conduct of clinical studies to national and international authorities and ethics committees Support in the protocol-compliant conduct of clinical studies, e.g. in Screening and enrollment of participants Conduct or accompaniment and documentation of study visits Organization and coordination of diagnostics and sample shipping Implementation of required protocol regulations Documentation in electronic databases Administration and maintenance of medical databases and support of hospital information systems Recruitment of participants and external centers Contract management and internal accounting Creation of statistics Creation of protocol-specific work instructions Communication with external cooperation partners

• Collection of data and reference findings and support of physicians in planning possible study participation
• Submission and conduct of clinical studies to national and international authorities and ethics committees
• Support in the protocol-compliant conduct of clinical studies, e.g. in
• Screening and enrollment of participants
• Conduct or accompaniment and documentation of study visits
• Organization and coordination of diagnostics and sample shipping
• Implementation of required protocol regulations
• Documentation in electronic databases
• Administration and maintenance of medical databases and support of hospital information systems
• Recruitment of participants and external centers
• Contract management and internal accounting
• Creation of statistics
• Creation of protocol-specific work instructions
• Communication with external cooperation partners

• We look forward to a team player with completed vocational training in a healthcare profession (e.g. medical documentarian), nurse and/or university degree as well as completed further training: Certification as Study Assistant according to the BÄK further training curriculum (120 hours) * or with equivalent skills and experience.
• Professional experience, especially in the field of study coordination and conduct, ideally with oncological studies, particularly radiooncology
• Ideally knowledge of third-party funding procedures
• Good German and English skills in writing and speaking
• Good IT skills (electronic data entry, MS Office)
• Experience in handling databases is an advantage
• Independent, result-oriented and structured working style
• Communication and team skills as well as high commitment
• *A completed further training as Study Nurse (at least 120 hours) leads to classification in salary group 9b TVöD/VKA. If this further training is not yet available, temporary classification in salary group 8 TVöD/VKA applies.