Hobson Prior is seeking a Clinical Research Coordinator for a part-time freelance role in Słupsk, Poland. This position focuses on supporting clinical trials through data management and verification. Our client is looking for someone to start as soon as possible for a 4-month contract, working 8 hours per week.

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

Responsibilities:

• Enter and verify data accurately.
• Resolve any data-related queries.
• Upload source documents.
• Monitor data related to adverse events (AE) and serious adverse events (SAE).

Key Skills and Requirements:

• Experience in clinical trials.
• Strong attention to detail for data entry and verification.
• Ability to manage and resolve data queries efficiently.

For more information, please contact Terrah-Leigh Pietersen.

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.

By providing your details and submitting this form you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates and those categories of third parties in our privacy policy at hobsonprior.com/privacy-policy.