Flexible Work, Better Balance
Work Schedule – Standard Office Hours, 40 hours per week
Environmental Conditions – Office
Job Description – Provide medical oversight of clinical trials, ensuring compliance with company SOPs, client directives, GCP and regulatory requirements. Attend investigator and sponsor meetings; provide medical consultation and support business development. Review and analyze serious adverse events, marketed products ICSR, and periodic safety reports (PBRER, PSUR, DSUR). Manage contracted services, support tumor and risk management activities, and maintain therapeutic training.
Key Responsibilities – General Support: Delegate tasks to PVG, adhere to regulations and SOPs, provide medical consultation and answers, deliver protocol training, contribute to CSRs, IND/NDA reports and other safety documents. Clinical Trial Support: Monitor safety variables, discuss medical concern...