Are you a dedicated individual looking to put your clinical expertise to work fully flexibly in a remote position?

Hobson Prior is seeking a Study Coordinator to support clinical research activities on a part-time freelance basis. This role is ideal for someone fluent in Dutch and based in The Netherlands. You will play a key role in ensuring the smooth operation of study-related tasks, with a focus on patient screening, data management, and reporting.

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

Responsibilities:

• Assist with identifying and screening patients for clinical studies.
• Enter and manage study-related data accurately.
• Document and report any adverse events (AEs) or serious adverse events (SAEs).

Key Skills and Requirements:

• Native-level proficiency in Dutch.
• Ability to work remotely from The Netherlands.
• Strong organizational skills and attention to detail.
• Familiarity with clinical study processes is beneficial but not mandatory.

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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