Study Coordinator (Denmark)

Hobson Prior are currently looking for a Study Coordinator to join a brilliant CRO on a contract basis located in Copenhagen. Our client is focused on maximising the speed and effectiveness for those who conduct clinical trials.

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

Key Responsibilities:

• For this role, you will serve as the main point of contact for CRAs and study supervisors.
• Organise and arrange patient visits.
• Manage data entries and query resolutions.
• Uphold study records throughout the study, which may involve IRB approval, continuing evaluations and any other reportable items.
• The ideal candidate will attend and contribute to supervising visits and audits when suitable.
• Responsible for sample collection and processing such as non-invasive processes.

Requirements:

• Fluency in the English and Danish languages.
• Willing to travel for business needs.
• Familiarity within data input.
• Acquaintance with Oncology.
• Knowledge on EDC system - iMedidata; IRT system - Suvoda; Lab Portal - PPD Preclarus, etc.

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.