TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.
The Study Nurse coordinates and manages clinical studies involving drugs, medical devices, and cosmetics under the supervision of the Principal Investigator (PI). Working closely with the TFS In‑house Clinic study team, this role ensures that all study activities are conducted in accordance with TFS policies, Standard Operating Procedures, Good Clinical Practice (GCP), and all applicable national and international regulations, including data protection requirements.
Coordinate, prepare, and conduct patient visits according to the study protocol, including screening support.
Prepare and maintain patient source documentation and enter data into electronic/paper systems.
Support SAE reporting, monitoring visits, audits, and inspections.
Support study start‑up activities, including feasibility, pre‑study visits, and site initiation.
Work experience as a Study Nurse (ideally 2+ years) or completed vocational training as a Nurse, Medical Documentation Assistant, Medizinische Fachkraft (MFA), or similar healthcare profession.
Very good command of written and spoken English.
Proficiency in MS Office applications.
We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. As a global CRO with the ultimate goal of ensuring patients’ safety and well-being, we provide biotechnology and pharmaceutical companies with tailored clinical development solutions.