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Location: Zürich
Start Date: ASAP
Our client is a Swiss biotech company pioneering next-generation vaccine technologies. With a strong focus on translational science and early clinical development, the company combines innovation and agility to address global infectious diseases.
Responsabilities
- Lead early-phase (I–II) clinical trials, ensuring delivery on quality, timelines, and budget
- Develop clinical and regulatory strategies in collaboration with the Clinical Director
- Manage CROs, vendors, and clinical sites to guarantee performance and compliance
- Oversee ethical/regulatory submissions and maintain data integrity across systems
- Analyze and present clinical data, contributing to study reports and cross-functional decisions
- MSc or PhD in Life Sciences with 5+ years’ experience in Pharma/Biotech clinical project management
- Proven record managing early-phase trials and external partners (CROs/vendors)
- Solid knowledge of ICH-GCP, risk management, and regulatory interactions (EMA, FDA, etc.)
- Strong planning, communication, and data interpretation skills
***Please forward your application should you meet the requirements above – applications which do not meet these requirements will not be considered***
headcount AG
Key Skills
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