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are able to quickly adapt to different multicultural teams and diverse concepts? Then our Clinical Development Postgraduate Training Program is a unique opportunity for you to discover the science of
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Role Requirements: • PhD in chemical biology, biochemistry, molecular or cellular biology, or related field. • Proficiency with immunoassay and proximity-based assay development (ex. ELISA, HTRF, TR
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What You'll Bring to the Role: • PhD or MD/PhD in neuroscience, genomics, cell biology or related field (PhD students in the last year of their thesis work, are eligible to apply). • A strong
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. This position reports to the Head Patient Safety Immunology. Key Responsibilities: • Providing expert safety input to the clinical development program for assigned projects/products, participating as an active
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sources through lifecycle management. YOUR KEY RESPONSIBILITIES: Your responsibilities include, but are not limited to: • Provides expert safety input to the clinical development program for assigned
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Role Requirements: • PhD in cell biology, medical science, computational biology or a related discipline (ideally a combination of wet lab and computational) PhD students in the last year of
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for preclinical support of clinical program-related scientific objectives. This includes assessment of medical need, proposal of clinical development pathways, and re-view of preclinical data for clinical
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Role Requirements: • PhD in Oncology, Molecular and Cellular Biology or related subject area (PhD students in the last year of their thesis work, are eligible to apply). • Hands on experience with
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science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity
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Primary Location: Barcelona, Spain (hybrid) Alternate Location: United Kingdom (remote) About this role: As our Global Program Safety Lead within the CRM therapeutic area you will provide scientific