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Job Description
I. Key Responsibilities:
Oversee safety evaluation and toxicology project management, liaising with domestic and international clients to discuss in vivo and in vitro experimental needs (including experimental design, challenges, and potential risks). Align on requirements and deliver tailored experimental proposals.
Execute efficient project management: Collaborate closely with laboratory teams, sales/business development (BD), and cross-functional departments to ensure projects adhere to predefined plans and timelines. Maintain proactive communication with clients on progress, and coordinate resources to resolve project-related issues.
Review experimental results and reports, providing clients with scientifically sound data interpretations. Organize and address client inquiries promptly.
Assist in preparing for client visits, audits, and regulatory inspections.
II. Qualifications:
Master’s or Ph.D. degree in Toxicology, Pharmacology, Pharmacy, or a related discipline.
Understanding of the drug research and development (R&D) process, with familiarity in toxicity evaluation platforms (e.g., in vitro assays, in vivo studies).
Strong learning agility, scientific rigor, and problem-solving skills.
Excellent communication, project management, and time management abilities, with resilience to thrive in fast-paced environments.
Proficiency in written and spoken English (listening, speaking, reading, writing) for effective workplace communication.