Willem J. Remme
Pat Illingworth
Karen Keukelaar
Jan A. de Witt
Karen J. Williams
Ralph Hultzer
Dori Kadmon
Regulatory Affairs
Clinical Monitoring
Pharmacovigilance
Clinical Event Management
Medical Review
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Scientific Advisory Board
Biography Dr Williams
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Clinical Research Associate

On time delivery of data which can be relied upon is essential in any clinical trial and good clinical research associates are needed in order to reach that goal. Surely, the CRA should have a clear understanding of the protocol, GCP/ICH guidelines, and their implication and have a bio-medical or other scientific background. Lots of experience if possible. But honestly, what really makes a good clinical research associate?

Job commitment certainly is a key component since it affects so many other qualities of the associate. It is always a challenge for a CRO to find the right people for the job.

However, commitment is also influenced by the company where the clinical research associate works. A positive learning environment with adequate support in the field from experienced clinical project managers and other colleagues reduces the learning curve and has a major impact on the associate’s knowledge and skills.

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