o Manuscript/regulatory/posters/abstracts writing, per-clinical & clinical development
o Designing, planning, conducting and supervising preclinical studies (Oncology & Immuno-oncology)
o Review of study protocols, SOPs, reports, analysis and interpretation of data
o Comprehensive profiling of novel discovery targets, safety aspects, SWOT analysis
o Preparation of scientific documents (e.g. literature publications, IND technical documents) and interaction with various external and internal interfaces.
o Molecular biology, in vivo pharmacological drug screening, early safety and toxicity studies
o Sound knowledge of pathophysiology and pharmacology of cancer
o Good understanding of cli...
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