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Responsibilities:
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.
Co-author 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
Requirments:
PhD and/or MD, strong scientific background in immunology or oncology, international Post-doctoral training is an advantage
Pharmaceutical industry R&D work experience is an advantage
Ability to analyze data, trouble-shoot, train and work closely with other functions
Good written, spoken and interpersonal communication skills in Chinese and English required.