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Director of Genetics Formulation is responsible for formulation development, project management, and team development.
The Executive Director of Biologics Production is responsible for the company’s overall manufacturing activities of biopharmaceuticals.
The Clinical Trials Liaison Officer is the primary point of contact among KELUN, investigators and the clinical trial sites
The Director/Head of Clinical Operation oversees the direction, planning, execution and interpretation of clinical trials/research activities.
The Director of Early Stage Clinical Development performs protocol design and implementation of projects in early phases of clinical trials.
The Clinical Strategy Lead provides strategic clinical directions for the life cycle of products as a representative of global clinical development.
The Late Stage Clinical Development Director leads clinical development planning, design, execution and reporting of late stage clinical trials.
The Director of Formulation Development is responsible for drug product formulation development/characterization.
Director of Biologics QA is responsible for building and managing a biologics QA team, establishing and maintaining quality assurance systems.
Director of Biologics Process Development is responsible for the large-scale production of biologics from mammalian cell culture.