04.04.24 | Vollzeit | Bern | SAKKAnd manage the study applications for the internal are responsible for the writing of international or national SAKK study are responsible for the project management of the study development; you create project plans, monitor the specified project goals (milestones
Später ansehen25.04.24 | Vollzeit | Bern | Randstad Schweiz AGAnd procedures are managed effectively. Requirements - Bachelor's or master's degree in technical or natural sciences. - Minimum 3 years of working experience within pharma or biotech. - Minimum 4 years of working experience with CSV. - Knowledge of FDA 21CFR part 11/EUGMP Annex 11 regulations and ISPE GAMP 5
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