Clinical project scientist
AllschwilCk Group
...Sound knowledge of the drug development process, trial-related regulatory requirements/ICH GCP guidelines. Fluent in English (written and spoken). [...]
Kategorie Recht
AllschwilCk Group
...Sound knowledge of the drug development process, trial-related regulatory requirements/ICH GCP guidelines. Fluent in English (written and spoken). [...]
Kategorie Recht
AllschwilCk Science
...Sound knowledge of the drug development process, trial-related regulatory requirements/ICH GCP guidelines. Fluent in English (written and spoken). [...]
Kategorie Recht