Perform on-site monitoring visits as well as site identification, feasibility and selection as required
Prepare project-specific support materials and templates in accordance with protocol and other specifications
Assist in the preparation and management of regulatory and ethics applications for clinical research studies as required
Ensure that all adverse events are reported in accordance with the required time frames for reportability
Previous experience working with pharmaceutical/biotech companies or CROs
Independent monitoring experience of a minimum of 2 years’
Fluent in English, German and Italian
Worked as a freelancer for a minimum of 1 year
0.5-0.6 FTE available
If you are interested in discussing this role in further detail, you can reach me on: +44 1273 952187 / email@example.com
Day / Hourly Rate: On application
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