25.04.24 | Teilzeit | Solothurn | Ypsomed AGParticipation. Ypsomade. In the area of Quality Management, Regulatory and Medical Affairs in Solothurn, we are looking for an experienced and passionate person to join the Medical Affairs team as a Scientific Services Manager 80 - 100% Ref. No. 6754 Location Solothurn Hybrid Support us
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
Später ansehen25.04.24 | Vollzeit | Corsier-sur-Vevey | Randstad Schweiz AGSupporting compliance activities (batch review, deviations, investigations.) - Participating in maintaining the functionality of the laboratories/clean rooms - Interacting with different stakeholders (e.g., Quality Assurance, Project Managers, or Operational team) Who are you? - You have a technician diploma
Später ansehen15.04.24 | Vollzeit | Basel (Basel-Stadt) | www.hays.chYour profile o Degree in a life science or health care discipline o Previous experience in clinical vendor management or similar role with focus on clinical research o Clinical Trial/Medical Affairs experience in a pharmaceutical company or a contract research organization is required o Experience
Später ansehen05.11.19 | Vollzeit | Schlieren | headcount AGTo become a permanent position. The main tasks include mostly organizing projects and leading the project managers, liaising with KOLs, protocol development, CRO selection and management. \ Accountable for the planning, implementation and execution of the clinical trial according to ICH, GCP and other
Später ansehen04.11.19 | Vollzeit | Zürich | Ava AGMore if you don’t hold a PhD Relevant experience in and/or knowledge of at least half of the areas below (by order of importance) - Managing and conducting Phase I-IV clinical trials according to GCP - Managing CROs from the sponsor side - Managing projects in clinical/medical settings - Writing
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