EPM is working with a CRO seeking a Clinical Trial Assistant in Hamburg for an exciting project.

• 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.

• 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.

Ciaran Gartland

Recruitment Consultant

email: ciaran.gartland@epmscientific.com