Career Opportunities
Study Director, Toxicology
Qualifications:
Minimum: MS in toxicology or related fields (e.g. medicine, physiology, biology) and 5-10 years experience in designing/conducting/monitoring toxicology studies. Excellent organizational, interpersonal, oral and written communication skills with high integrity and team-oriented mentality. Preferred: DVM/MD or PhD in toxicology or related disciplines with more than 7 years experience in the pharmaceutical/ biopharmaceutical industry or contract research organizations. Board certification in toxicology and fluency in Chinese are desirable. Knowledge of GLP regulations and relevant FDA and ICH, guidelines for nonclinical safety testing is highly desirable. Excellent written and oral communication skills.
Responsibilities:
This position is responsible for the overall planning and conduct of non-clinical investigations, in accordance with applicable regulatory guidelines and contemporary scientific practice. Responsibilities is included but not limited to: Protocol design, IACUC submissions, study initiation and documentation, data analysis and interpretation, regulatory compliance, as well as reporting of study results. He/she will act as a key point of contact for all internal departments engaged in a study and develop strong working relationships with relevant external representatives to ensure the smooth flow of data to the client organization. This individual must pay attention to details, check that all data is appropriately recorded and compiled throughout the study, and accurately interpreted and documented in subsequent reports, and ensure that all studies are conducted in-line with GLP guidelines and regulatory test standards. You should have the ability to handle multiple studies and solve issues arising on a dedicated study. This position also requires direct communications with Sponsors and an ability to work across functional units internally to plan, execute, and complete testing programs that meet Sponsor requirements and ensure to deliver on-time high quality reports to clients.
WuXi AppTec welcomes overseas talents join us. We offer you a highly competitive compensation and full benefits package along with an exciting world-class work environment. For more information, please visit our website: http://www.wuxiapptec.com/ .
For prompt consideration, please send your CV to: szhr@wuxiapptec.com
WuXi AppTec Co., Ltd. is a NYSE listed public company based in Shanghai, China. We offer global pharmaceutical/biopharmaceutical companies diverse outsourcing services in combinatorial, medicinal, synthetic chemistry and manufacturing of API’s and finished drug products for preclinical and clinical trials. Our clients include over 80 leading global pharmaceutical and biotech companies in the U.S., Europe and Japan.