Study Coordinator (m/f/d) Clinical Trials (Physician)

Start in our team

Join our team and support our principal investigators in conducting clinical trials at the earliest possible date. The position is initially limited to one year.

What we offer you:

• Classification in pay group E 8 TV-L, provided collective agreement requirements are met
• Full-time employment, currently 38.5 hours / week; part-time employment may be possible within the framework of certain working time models

• A plus for employees and the climate: NAH.SH Jobticket with the highest discount level
• Many attractive employee discounts on various online platforms and with various companies

• Further exciting benefits of UKSH can be found here:

What awaits you:

• Preparation and coordination of study visits, diagnostics, and laboratory work according to the study protocol
• Processing and documentation of study-relevant data in CRFs as well as handling queries; if necessary, also drug accountability

• Preparation and support of initiations, monitoring visits, audits, and regulatory inspections
• Administration and archiving of all study documents and materials

What you bring with you:

• Completed training as a Medical Documentation Assistant or a comparable medical training, possibly with further training as a Study Nurse
• Experience in conducting clinical Phase II, III, and IV studies

• Good knowledge of ICH-GCP, AMG, and MDR
• Proficient handling of English-language documents and study protocols as well as English correspondence

• An independent and structured way of working, reliability and organizational talent, as well as communication skills and enjoyment of working in a team

We look forward to receiving your application by 01.07.2026, stating the vacancy number 26542.