Paramount Clinical Research: Clinical Research Associate II (CRA) – Netherlands, great company!
An international Clinical Research Organisation (CRO) is currently looking for a Clinical Research Associate (CRA) to join their team in the Netherlands. It’s a great company with a global reach and the CRA will be joining an experienced team. You will have flexibility in your role to work from home, coupled with excellent training to help move your career forward! This is an opportunity not too be missed.
As a Clinical Research Associate (CRA), you will identify, select, initiate and close-out appropriate clinical studies. The Clinical Research Associate (CRA) will monitor studies according to the companies SOPs, ICH-GCP and regulatory requirements. They will also benchmark for less experienced team members. Other aspects of the role include preparing regulatory submissions, coordinating document translation, maintain study documents, and also act as a lead on certain studies while mentoring less experienced team members.
To be considered and work as a Clinical Research Associate (CRA) it is essential to have experience monitoring clinical trials on an international level. A scientific, medical or related qualification is essential coupled with local and English language. Strong communication skills, excellent knowledge of ICH-GCP and EU guidelines plus flexibility are essential for this role.
This is a great chance to work for a company that is at the forefront of clinical research, and they will help you develop your experience and give you a chance to work on new, exciting studies!
For full job details please call Gareth on +44 (0)121 616 5135 or apply now!
Keywords - clinical, clinical research, clinical research associate, senior CRA, senior clinical research, clinical trials, clinical study, clinical studies, clinical associate, clinical monitor, CRA
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