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Job Responsibility:
1. Working with the liner manager in managing strategic projects and tasks, including aspects of project planning, resourcing, process management, risk assessment,and cross-functional communications;
2. Support BDs and clients for designing pharmaceutical toxicity studies to meet the clients’ needs;
3. Communicating and reviewing the quotations for the toxic package with quotation team, and communicate the quotation with clients;
4. Deeply involve in new project launch readiness planning, resource management, and cross-functional collaborations;
5. Play an active role in the ad-hoc risk management of the project and ensure efficient communication;
6. Build and maintain a strong relationship with stakeholders and cross-functonal teams.

Requirements:
1. Master or above degree in toxicology, pharmacology related biological or medicine degree;
2. Fluent in English (written and verbal); overseas study/work experience is preferred.
3. Familiar with FDA/OECD/NMPA regulations and GLP compliance.
4. 5+years of project management experience in biopharmaceuticals; expertise in small-molecule drug safety assessment is a plus.
5. Proven ability to manage complex projects and facilitate cross-functional collaboration with strong communication skills.
6. Team-oriented with adaptability to cross-departmental and cross-regional work environments.