Accountabilities :

• Manage study timelines, objectives and budgets, ensure data accuracy and integrity.
• Analyze and interpret the data generated during discovery, early and/or full development; responsible for timely and effective communication of data, strategy and results to the project teams.
• Identify potential project hurdles, suggest solutions and contribute to contingency plans.
• Coauthor and prepare key preclinical and clinical, and regulatory documents, scientific manuscripts and patent application, including, but not limited to: study protocols, study reports, modeling reports, investigator brochures, IND/IMPDs and NDAs within agreed timelines, and meeting all regulatory requirements.
• Works collaboratively within cross-departmental teams, department-wide initiatives and work streams.
• Provide cell therapy expertise on due diligence of BD projects and prepare appropriate documentation.
• Adhere to the appropriate SOP and GxP guidelines, and embrace a collaborative culture
  

Qualifications:

• PhD and/or MD, strong scientific background in immunology or oncology, international Post-doctoral training is an advantage.
• Have antibody discovery and characterization experience.
• Could do virus vector design and optimization
• He/she is familiar with in vivo animal study, could evaluate drug potency and safety.
• Extensive knowledge of cell biology and cancer biology, solid scientific publication.
• Pharmaceutical industry R&D work experience is an advantage

上班地址：康南路222号