Clinical Research Coordinator

Eblex Group; Erlangen; Vor Ort; EUR 83.000 - 124.000; Teilzeit

Zusammenfassung

Eblex Group is seeking a Freelance Clinical Research Coordinator to support a Phase I trial in the Erlangen area. The role is a flexible freelance assignment with about 1 day per week (0.1 FTE ad-hoc), focusing on study coordination rather than patient procedures.

You will assist with recruitment timelines, study deliverables and on-site coordination, including informed consent discussions and logistics. German fluency is required and attendance at the Erlangen site will be needed as required.

Qualifikationen

• Previous experience coordinating clinical studies at an investigative site, hospital or clinical research centre.
• Experience with eCRF systems and clinical study data entry.
• Experience supporting informed consent processes and participant communication.
• A good understanding of clinical study processes and GCP requirements.
• Strong organisational skills and the ability to work independently.
• Fully fluent German.
• Availability to attend the Erlangen site when required.

Aufgaben

• Supporting patient information and informed consent discussions.
• Following up on study logistics and sample management.
• Coordinating site activities to support study timelines.

Kenntnisse

Clinical study coordination

eCRF experience

GCP knowledge

German fluent

Independent worker

Tools

EDC systems

Jobbeschreibung

Freelance Clinical Research Coordinator | Phase I

Department: Clinical Research / Clinical Operations

Contract Type: Freelance / Contract

Duration: July 2027

Capacity: 1-day p/w (0.1 FTE ad-hoc)

Overview

We are supporting a Phase I clinical trial site in the Erlangen area that requires an experienced Clinical Study Coordinator on a flexible freelance basis.

The coordinator will provide on-site support to help the study team stay on track with recruitment, timelines and study deliverables.

The commitment is expected to be around 8-hours per week, so it may suit someone looking for a small freelance assignment alongside their existing work.

This is a study coordination role, not a Study Nurse position. It does not involve performing patient procedures or clinical assessments.

Key Responsibilities

• Supporting patient information and informed consent discussions
• Following up on study logistics and sample management
• Coordinating site activities to support study timelines

Required Experience & Skills

• Previous experience coordinating clinical studies at an investigative site, hospital or clinical research centre.
• Experience with eCRF systems and clinical study data entry.
• Experience supporting informed consent processes and participant communication.
• A good understanding of clinical study processes and GCP requirements.
• Strong organisational skills and the ability to work independently.
• Fully fluent German.
• Availability to attend the study site in the Erlangen area when required.

Desirable (Nice to Have)

• Experience supporting Phase I clinical trials.