Site Management Associate I or II

Hemalatha Jaganathan
Flexible for Home based applications
upto 30000 EUROS
Closing date
9 Oct 2020

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Clinical Research, Clinical Operations
Full Time
Contract Type
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Job Profile

The Site Management Associate I/II (SMA I/II) is responsible for managing, implementing and monitoring clinical studies, with support, in a team setting according to ICON SOPs, SSPs and all applicable rules and regulations.  The responsibilities of this position include, but are not limited to:

  • Identifying, training/initiating and closing out German or French or Dutch study sites.
  • Conducting remote site monitoring visits and/or targeted on-site visits as needed.
  • Conducting remote site management activities.
  • Managing study sites and the required protocols, amendments and/or deviations, assuring that data is reported accurately and timelines are maintained. 
  • Travel up to 25% of your time.

Required Skills

  • A Bachelor’s degree in the life sciences, expertise with regulatory guidelines and clinical terminology, and demonstrable strong site management experience will ensure your success on our team. 
  • You will need to have fluent written and spoken Local (German or French or Dutch) language and English skills. 
  • We would also welcome some previous experience as a CRA or an In- house CRA.
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