Study Coordinator / German-speaking

Hobson Prior; Deutschland; Remote; EUR 30.000 - 40.000; Teilzeit

Zusammenfassung

A leading life sciences recruitment agency is seeking a Study Coordinator to work remotely from anywhere in Germany. This part-time freelance role involves supporting clinical studies through patient coordination and data management to ensure high quality and compliance. Key responsibilities include screening patients, data entry, and monitoring study visits. The ideal candidate will have experience in clinical research processes and excellent organizational skills.

Qualifikationen

• Proficient in clinical research processes and medical terminology.
• Strong organizational, communication, and time management skills.
• Ability to troubleshoot and navigate clinical technologies effectively.
• Knowledge of patient safety reporting and escalation procedures.
• Experience in fostering positive relationships with patients and research teams.

Aufgaben

• Help screen patients for participation in clinical studies.
• Enter data into relevant systems and maintain accurate records.
• Document and report any adverse events (AEs).
• Coordinate scheduling and logistics.
• Ensure informed consent is properly obtained.

Kenntnisse

Clinical research processes

Organizational skills

Communication skills

Time management

Troubleshooting clinical technologies

Relationship building with patients

Jobbeschreibung

Overview

Are you a dedicated individual looking to put your expertise to work fully flexibly in a remote position? Hobson Prior is seeking a Study Coordinator to be based anywhere in Germany. This part-time freelance remote role involves supporting clinical studies by coordinating patient activities, managing data, and ensuring study documentation is accurate and complete. You will play a key role in delivering a positive experience for patients and research teams while maintaining high-quality standards.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities

• Help screen patients for participation in clinical studies.
• Enter data into relevant systems and maintain accurate records.
• Document and report any adverse events (AEs) or serious adverse events (SAEs).
• Coordinate scheduling, logistics, and communication between patients, investigators, and other study-related entities.
• Ensure informed consent is properly obtained and documented.
• Monitor study visits and ensure all data is entered into systems within required timeframes.
• Build strong relationships with patients, investigators, and research teams to enhance the study experience.
• Perform quality checks to ensure data integrity and compliance.
• Support query resolution and assist with inspection readiness.
• Manage payments for study assessments as needed.
• Adhere to training requirements and system access guidelines.

Qualifications

• Proficient in clinical research processes and medical terminology.
• Strong organizational, communication, and time management skills.
• Ability to troubleshoot and navigate clinical technologies effectively.
• Knowledge of patient safety reporting and escalation procedures.
• Comfortable working remotely with occasional travel (less than 10%).
• Ability to analyze study protocols and identify key outcomes.
• Experience in fostering positive relationships with patients and research teams.

For more information, please contact Terrah-Leigh Pietersen.

If you are interested in applying to this exciting opportunity, then please click Apply or visit the Contact Us page to speak to one of our specialists.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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