臨床開發專案管理, Department of Clinical & Regulatory (Title commensurate with experience)

We are seeking a drug development professional to join TaiMed's Clinical Development & Regulatory Affairs team.

Play a key role in advancing innovative therapies through clinical development and regulatory pathways.

• Facilitate the clinical development of new drugs (biologics) from early- to late-phase studies.

• Ensure efficient project execution with CROs, including budget, timeline, and quality management.

• Strong understanding of and compliance with GCP.

• Coordinating communication among internal teams and external partners, many of whom are international. **Strong English communication skills REQUIRED **

• Study scientific literature, clinical guidelines, and global regulatory requirements for drug development.

• Other related tasks assigned by the supervisor.

• Title depends on experience.