Sr Site Management Associate

The Senior Site Management Associate 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 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.
• Some monitoring in Belgium
• National travel up to 25% of your time.

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. We would also welcome some prior Study Start Up experience ie study feasibility, site identification, ethics committee and regulatory authority submissions, contract negotiations, site activation.

You will need to have fluent written and spoken Local (Dutch) language and English skills. This would be a great opportunity for someone with the skills and background like an inhouse CRA / remote monitoring CRA.