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.

Salary:

€60.00 – €70.00/Hour

For more information, please contact James Inwood.

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.

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