Study Coordinator / German-speaking

Hobson Prior International Ltd; Frankfurt; Remote; EUR 40.000 - 60.000; Teilzeit

Zusammenfassung

A leading life sciences recruiter is seeking a dedicated Study Coordinator for a part-time freelance remote role based in Germany. The successful candidate will coordinate patient activities, manage data, and ensure study documentation is accurate. This position requires strong proficiency in clinical research processes and excellent communication skills. Candidates must have the right to work in Germany and be comfortable working remotely with occasional travel.

Qualifikationen

• Proficient in clinical research processes and medical terminology.
• Strong organizational, communication, and time management skills.
• Experience 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.
• Coordinate scheduling and communication between patients and investigators.

Kenntnisse

Clinical research processes

Medical terminology

Organizational skills

Communication skills

Time management

Troubleshooting clinical technologies

Patient safety reporting

Analytical ability

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.

Hobson Prior is seeking a Study Coordinator to join a part-time freelance remote role, based in Germany. This position 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.

Key Skills and Requirements

• 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 to speak to one of our specialists visit the 'Contact Us' page.

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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