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Upsilon Global, Uppsala
Unlike some CRO contracts in which you’re required to save a failing study or recruit for struggling sites, our client insists on only entering clinical study agreements from start-up phase, meaning you’ll be responsible for studies full-cycle, from start-up through to close-out, utilising all aspects of your clinical research experience.
- Perform all types of site visits including, but not limited to, qualification visits, initiation visits, monitoring visits, motivational visits, audit support visits, and termination visits.
- Assist with document submissions to local authorities
- Ensure that all study related communication including e-mail is tracked, printed and filed as required
Publicerad 7 augusti
Berlitz Corporate Language Services is looking for free-lance English Language Teachers (EFL) to teach general and professional English to...
Berlitz International Sweden AB, Stockholm
Platsbanken AMV, 15 augusti