Studiendokumentarin / Studiendokumentar (w|m|d)
Core
Document clinical trials and support their organization and execution in a certified center for hematological neoplasms.
Role type
Clinical trial documentation specialist
Builds
Clinical trial data and documentation for hematological and oncological research
Domain
Healthcare / Clinical Research / Hematology & Oncology
Required skills
Clinical trial documentation, Study audit organization, Clinical data management, Data submission to registries, Knowledge of GCP principles, Knowledge of pharmaceutical regulations, Medical background (MFA or Study Nurse), Experience with clinical trials
Preferred skills
Experience in allogeneic stem cell transplantation, Acute leukemia, Multiple myeloma, Lymphoma
Technologies
Clinical trial management systems, Electronic data capture tools
Responsibilities
Document clinical trials, Organize and accompany study audits, Manage and archive study data, Submit study data to national and international registries, Participate in studies for stem cell transplantation and hematological malignancies
