職位描述
職位描述：
Job Description
- To propose preclinical strategies, design and coordinate appropriate preclinical studies, primarily PK, PKPD, BioAnalytical, and Tox to support preclinical development of drug candidates mainly biologics to successfully IND filing
- To implement studies in preparing protocols, monitoring study progress, analyzing data and writing reports and regulatory documentation and reporting to the client or integrate project team.
- To conduct extensive reference search and information collection of recently science advancement and report/present to the manager and project team.
- To coordinate cross-functional effort (Discovery, Pharmacology, CMC, Registration and business partners) in planning budgets, timelines and resource allocations
- To participate meeting and teleconference with global clients/team members during after work hours
- To thrive in a fast paced science-driven environment and collaborate with people with diverse backgrounds. He/she might be expected to contribute to the scientific direction of this group, mentoring the staff, and nurturing technological innovation.
- Might supervise and team build team, depending upon qualification, a group of SDs
Requirement
- A MD, MS or Ph.D in toxicology, biochemistry, biology, or life-science related discipline is required.
- Knowledgeable in fundamental toxicology, large molecule discovery and development
- Prior experience in animal study and/or biology assay and well understanding of in vivo system, bioanalytical assay (LBA), PK is highly expected
- Excellent interpersonal and communication in both Chinese and English
- Prior experience in preclinical development in life science industry is a big plus
- Strong collaborative skills and ability to work in a team environment expected
