Stellenbeschreibung
About us EPM is working with a CRO seeking a Clinical Trial Assistant in Hamburg for an exciting project. Tasks Guarantee the integrity, completeness, and high quality of clinical data gathered from study sites. Oversee the organization and maintenance of essential documentation, including Trial Master Files (TMF) and Investigator Site Files (ISF). Manage logistical aspects of the study, such as coordinating the delivery of materials, handling documentation, and overseeing shipment processes. Provide operational support across various functions, including financial tracking, translation coordination, and progress reporting. Contribute to the planning and execution of key clinical trial meetings, including investigator and internal team sessions. Profile Strong (3 years preferred) experience in clinical research (CRO, biotech, pharma, or clinical research unit). Willingness to work in the office 4-5 days per week. Fluency in German and English is essential. Contact Ciaran Gartland Recruitment Consultant email: ciaran.gartland@epmscientific.com