Make your mark in global health by managing high-impact clinical trials with a leading CRO.

Hobson Prior is seeking a Clinical Research Coordinator to join a hospital site in Poznan, Poland, on a part-time freelance basis. This role involves supporting clinical research activities with a focus on data management and monitoring. The position is for a 6-month contract with an immediate start.

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

Responsibilities:

• Enter and verify clinical trial data accurately.
• Resolve queries related to data discrepancies.
• Upload source documents into the system.
• Monitor and review adverse events (AE) and serious adverse events (SAE).
• Ensure compliance with clinical research protocols and guidelines.

Key Skills and Requirements:

• Proficient in handling clinical trial data and resolving queries.
• Experience in data verification and monitoring processes.
• Ability to upload and manage source documents effectively.
• Native Polish speaker with strong communication skills.
• Availability to commit 20 hours per week for the duration of the contract.

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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