Clinical Research Coordinator

An experienced Oncology Clinical Research Coordinator looking for a flexible, long-term assignment where your expertise can make a direct impact on an important mCRPC study?

We are looking for an experienced Senior Clinical Research Coordinator to provide ongoing, flexible support to a clinical research site in Ghent, Belgium.

The assignment will support an oncology study focused on metastatic castration-resistant prostate cancer (mCRPC) and would suit an experienced clinical research professional who is comfortable working independently and can quickly integrate into an established site environment.

This is a particularly flexible opportunity, requiring approximately one day of support per month, making it well suited to an experienced freelancer or consultant looking to complement their existing workload with a long-term assignment.

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

Responsibilities:

You will provide hands-on clinical trial support to the site, with responsibilities including:

• Clinical trial data entry and maintenance
• Reviewing and resolving data queries
• Supporting source data verification and data quality activities
• Ensuring clinical trial data is complete, accurate and entered within required timelines
• Reviewing study documentation and identifying discrepancies or missing information
• Working closely with site personnel to resolve outstanding data and documentation issues
• Supporting the site in maintaining high standards of study compliance and data quality
• Providing experienced, independent support with minimal supervision

Key Skills and Requirements:

Given the nature of the assignment and the limited number of hours required each month, we are looking for a senior-level clinical research professional who can operate effectively from the outset.

The successful candidate should have:

• Strong clinical research experience within a site, hospital, CRO or pharmaceutical environment
• Previous experience supporting oncology clinical trials
• Strong clinical trial data entry and query resolution experience
• Experience with data verification and clinical trial documentation
• A good understanding of ICH-GCP and clinical trial processes
• The ability to work independently and manage priorities with limited supervision
• Strong attention to detail and a high level of accuracy
• Experience specifically within prostate cancer, metastatic disease or mCRPC studies would be particularly valuable.

For more information, please contact James Inwood.