Responsibility:
1. Design, conduct, and manage in vitro and in vivo experiments to evaluate the ADME and PK profiles of candidates in supporting of small molecular drugs development.
2. CRO management and coordination to ensure the bioanalytical work is performed in accordance with study protocols, work plans, SOPs and GLP guidelines.
3. Deliver and present experimental results in a timely manner to cross-functional project teams and at company project meetings.
4. Responsible for the review and interpretation of DMPK and bioanalytical data and relevant documents.
5. Prepare DMPK and bioanalytical data packages to support regulatory submissions. 6. Responsible for contract negotiation, development, and track for DMPK and bioanalytical studies.
7. Serve as QC officer on GLP activities related to Bioanalytical as required.
Qualification：
1. Bachelor's degree or above in DMPK or Bioanalytical or equivalent disciplines with 5 years of relevant working experience.
2. Experience working with external contract research organizations.
3. Excellent verbal and written communication skills.
4. Good interpersonal and team-building skills, including demonstrated experience working in a team environment.