Our client is is a premier life science service provider from worldwide which offers comprehensive research, development, and manufacturing service capabilities throughout the drug discovery, preclinical, clinical development, and commercialization process for small molecules, biologics, and CGT products. With over 20,000 employees, and operations in Worldwide, it has an excellent track record in the delivery of R&D solutions to its partners in North America, Europe, Japan and China.
This role is responsible for:
- Lead a team of toxicology focused on safety evaluation of biologics and provide related service to global clients.
- Provide leadership and scientific support for the preclinical studies of biologic compounds for sponsors'regulatory submissions.
- Oversee the activities and functions of the department.
- Work with Study Directors and technical teams to ensure studies to be conducted properly to meet timelines and in compliance with GLP regulations.
- Mentor Study Directors and technical leaders.
- Work with BDs and Sponsors in proposals and study designs.
Who we are looking for:
- Ph.D. in toxicology, pharmacology, medicine, veterinary medicine, or related field
- 10+ years'preclinical toxicology experience with biologics, experience in GLP preferred
- Excellent management, leadership and organization skills, able to establish good teamwork
- Excellent professional ethics, strategic thinking and innovation ability
- Excellent presentation and communication skills in both Chinese and English.
We Offer
A competitive remuneration package and a comprehensive benefits program will be offered to the successful candidate, reflecting the importance of this role within our organization.
We are looking for Scientists from global, we can provide working permit if it is needed.
How to Apply:
Interested candidates should submit their detailed resume with cover letter to