clinical study administrator in Neuchatel

Laura Deola, Basel Professionals Health Care & Life Sciences
job type
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job details

neuchatel, neuchâtel
life sciences
job type
reference number
laura deola, basel professionals health care & life sciences
058 201 55 50

job description

Randstad Professionals is looking for a Clinical Study Administrator for a major client in the tobacco industry based in Neuchâtel.


Your tasks would be:

  •  Management of the Study Master File and support to Study Managers during conduct of assessment studies including set-up, maintenance of paper and/or electronic SMF 
  • Regular quality control of the SMFs to verify completeness and to check that CROs/sites and external vendors file documents as per agreed SMF structure

  • Provide support in follow-up of invoices related to assessment studies conduct including the quality control of invoices against contracts as per work instructions and in agreement with Study Managers approve and file all invoices

  • Support to Study Teams including co-ordination of reviews of SMFs by all functions involved in study conduct


If you are interested to take on these responsibilities you should have the following requirements:

  • 1-2 yrs experience with Electronic Document Management System and/or electronic Study Master Files from pharma industry 

  • Experience in clinical studies

  • Good knowledge of MS Office Suite, capacity to learn the use of other IT tools

  • Good knowledge of Good Clinical Practice (GCP)

  • Fluent English, knowledge of other languages is an advantage.


If you are willing to learn new things and interested in new technologies we are waiting for you. We are looking forward to receiving your online application.

Please note a Swiss Work permit or EU-citizenship is mandatory for this position.