This position will be a key member of the R&D team supporting multiple areas including toxicology, bioanalytical sciences, PKPD and clinical pharmacology. S/he may also be as a primary representative on program teams and in collaboration and interaction with other functions in across development programs.
1.Develop and implement nonclinical safety strategies, design toxicology studies, author regulatory documents.
2.As a member of an integrated project team, interact with internal and external partners, and as well as regulatory agencies.
3.Ensure high scientific standards in conducting and reporting of nonclinical safety and investigative toxicology studies, and working with research project teams to utilize and interpret animal models of diseases for efficacy assessment and PK/PD evaluation
4.Manage studies at CROs and monitor to ensure high quality deliverables of the safety studies.
5.Work with the senior management to manage the departmental budget and resource.
1.PhD in biology, toxicology or related field and/or DVM, MD
2.Board certification in toxicology and / or pathology is highly desirable
3.10+ years in preclinical safety assessment of novel therapeutic entities
4.Knowledge and experience on GLP compliance and relevant ICH & FDA guidance documents
5.Experience in interfacing a preclinical function with QA, bioanalytical sciences, regulatory affairs, CMC, and clinical development functions
6.Excellent interpersonal skills and communication skills
7.Results oriented with strong problem-solving ski
一家大型制药集团，该集团产品主要集中在肿瘤，CNS，风湿免疫等领域；整个临床团队属于高大上的那种，多名华裔及海归，成员均来自500强，目前进入临床的项目大约10多个。该职位要求必须有巨头总部工作经验（欧美）
