Safety Pharmacology SD

To be negotiated

Education:

Master's degree

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Work experience:

3-5 years

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Number of positions available:

1


Job Description

  Job Responsibilities: Fully responsible for the operation and management of experimental projects; develop and rigorously implement experimental protocols; analyze and interpret research results, and prepare summary reports; execute Standard Operating Procedures (SOPs), and promptly propose suggestions for revising or supplementing relevant SOPs; keep abreast of the progress of research activities, review various experimental records, and ensure their timeliness and accuracy; promptly document any deviations that occur during the study and conduct thorough assessments, taking corrective actions when necessary; promptly address issues raised by the Quality Assurance Unit (QAU) to ensure compliance with all requirements at every stage.

  Job Requirements: Master’s degree or above in pharmacology, toxicology, clinical pharmacology, veterinary medicine, or a related field; familiar with GLP regulations and relevant technical guidelines; more than 3 years of experience in managing safety pharmacology projects at a GLP-compliant institution; strong communication and coordination skills; and excellent analytical and problem-solving abilities.

  Salary and compensation: To be discussed.

  Benefits and Perks: Six social insurances and one housing fund, free lunch, shuttle bus, on-site accommodation, employee health checkups, holiday benefits, birthday gifts, and more.