Hobson Prior is seeking a Clinical Study Coordinator to join our client's team. In this role, you will play a key part in designing and managing clinical studies. You will work closely with various teams to ensure the smooth execution of study protocols and oversee the entire process from site selection to data management. Regular travel is required for this position.

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

Responsibilities:

• Help design clinical studies and draft study protocols.
• Work with teams to select and train clinical study sites.
• Coordinate with labs and vendors for study needs.
• Manage budgets and approve invoices related to studies.
• Set up contracts with clinical sites and vendors.
• Ensure study supplies are organized and available.
• Oversee study monitoring and review data after studies close.
• Provide support to the product development team.
• Develop and implement policies and procedures for studies.
• Update team leads on study progress.

Key Skills and Requirements:

• A degree in a relevant field or equivalent experience.
• Strong skills in analysis and organization.
• Excellent communication skills, both written and verbal.
• Understanding of study protocols and data collection methods.
• Experience in managing or monitoring clinical studies.

For more information, please contact Elliot Croft.

Apply now

If you are interested in learning more or applying to this exciting opportunity then please click 'Apply' and upload a copy of your CV. Alternatively for further details or to talk directly to a life sciences recruitment specialist directly please select 'Contact me' at the top of this 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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