Preclinical development Manager

• Oversee the design and management of pre-clinical studies (GLP and non-GLP) for inclusion in regulatory documents, including PoC, pharmacology, toxicology, and biodistribution studies
• Manage contract research organizations (CROs) and external collaborations to support pre-clinical development programs
• Work closely with other functional areas and colleagues to ensure that all pre-clinical studies are performed in a quality, timely and scientific manner
• Write and edit preclinical study plans and reports
• Oversee drafting of preclinical sections for IB/IMPD
• Ensure compliance with global pre-clinical studies regulatory guidelines

• Ph.D. in biological sciences
• FELASA C accreditation
• Strong knowledge of biologics pre-clinical drug development and EMA/FDA/PMDA requirements (toxicology, biodistribution) is essential
• Experience managing direct reports, CROs, and external collaborations
• Minimum 3+ years’ experience in biotech/industry setting
• Excellent written and oral communication skills
• Fluency in English & French, all other language is an added value

• Challenging projects based on your interests and skills
• Personal follow-up and clear, transparent communication both before and after commencement of employment
• Possibility to follow extra training
• Inspiring network events and legendary after work drinks
• Strong network of industry leading clients
• Expertise within IT, Engineering and Life Sciences
• A flying start for every junior, growth opportunities and possibility to share gathered knowledge for more senior employees

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