Study Director - General Toxicology

As a Study Director, you will serve as the single point of scientific, administrative, and regulatory control for the study. Your key responsibilities will include: - Participating and overseeing all study activities such as animal dosing, clinical signs observation, data collection, and data analysis in compliance with applicable regulations, OECD Principles of GLP, and relevant SOPs. - Operating, maintaining, and using relevant equipment/instruments like centrifuge, laminar air flow, anesthetic machine, weighing balances, refrigerator, deep freezers, syringe pumps, etc. - Preparing and revising SOPs applicable to in vivo and in vitro experiments/procedures. - Communicating critical information to key study personnel, the sponsor, and responsible scientists as necessary. - Authorizing amendments and deviations to the study plan when applicable. - Responding to QA findings and resolving them promptly. - Approving study plans, amendments, and study reports. - Ensuring the timely archival of the study in accordance with current practices. Additionally, you will be responsible for all duties as a Study Director in alignment with the applicable SOPs.,