Clinical Research Nurse - Fluent german

Resourcing Group; Freiburg im Breisgau; Sur place; EUR 42 000 - 64 000; Plein temps

Résumé du poste

Resourcing Group in Freiburg im Breisgau, Germany, seeks a Clinical Nurse to recruit, screen, enroll, and support participants in clinical studies in collaboration with investigators. You will plan, coordinate, conduct, and document visits per approved protocols and perform essential clinical procedures.

Maintain research data in eCRFs, ensure GCP compliance, and coordinate with sponsors, CROs, and laboratories. Fluent German and English and office-based work are required.

Qualifications

• Min 2 years of Experience as a Clinical Nurse.
• Fluent in German and English.
• Office-based role.

Responsabilités

• Recruit, screen, enroll, and support participants in clinical studies in collaboration with investigators.
• Plan, coordinate, conduct, and document clinical study visits according to approved protocols.
• Perform clinical procedures such as blood collection, ECG recording, vital‑sign monitoring, and sample processing within professional scope.
• Collect, enter, verify, and maintain accurate clinical trial data in research databases and eCRFs.
• Ensure compliance with study protocols, GCP requirements, SOPs, ethical approvals, and applicable regulations.
• Prepare and maintain study documentation, participant records, and essential trial files.
• Coordinate study activities with principal investigators, sponsors, contract research organizations (CROs), monitors, laboratories, and other healthcare professionals.
• Manage study-related samples, laboratory materials, and investigational medicinal products according to study protocols and applicable procedures.
• Report adverse events, serious adverse events, protocol deviations, and other relevant findings according to established requirements.
• Support study start‑up, including preparation of documentation, ethics submissions, and coordination with sponsors.
• Assist with monitoring visits, audits, inspections, and study close‑out activities.
• Maintain participant confidentiality and promote patient safety throughout the research process.

Connaissances

German language

English language

Clinical study coordination

Data entry & documentation

Formation

Nursing diploma / Registered Nurse

Description du poste

• Recruit, screen, enroll, and support participants in clinical studies in collaboration with investigators.
• Plan, coordinate, conduct, and document clinical study visits according to approved protocols.
• Perform clinical procedures such as blood collection, ECG recording, vital‑sign monitoring, and sample processing within professional scope.
• Collect, enter, verify, and maintain accurate clinical trial data in research databases and eCRFs.
• Ensure compliance with study protocols, GCP requirements, SOPs, ethical approvals, and applicable regulations.
• Prepare and maintain study documentation, participant records, and essential trial files.
• Coordinate study activities with principal investigators, sponsors, contract research organizations (CROs), monitors, laboratories, and other healthcare professionals.
• Manage study-related samples, laboratory materials, and investigational medicinal products according to study protocols and applicable procedures.
• Report adverse events, serious adverse events, protocol deviations, and other relevant findings according to established requirements.
• Support study start‑up, including preparation of documentation, ethics submissions, and coordination with sponsors.
• Assist with monitoring visits, audits, inspections, and study close‑out activities.
• Maintain participant confidentiality and promote patient safety throughout the research process.

Requirements

• Min 2 years of Experience as a Clinical Nurse or Nurse
• Fluent in German and English
• office based