CAREERS
Associate Director, Preclinical Development
This individual will be responsible for the following key areas related to the selection and advancement of novel drug candidates: (i) Design of appropriate preclinical toxicology and ADME studies for new development candidates in accordance with regulatory requirements and current industry practices; (ii) Design, placement and management of toxicology, safety pharmacology, and ADME studies internally and at CROs; (iii) Interpretation and reporting of study data to internal and external working groups, including corporate management and clinical development teams; (iv) Preparation of study reports and regulatory documentation (US and Europe); (v) Selection and management of CRO’s.
The ideal candidate will hold a Ph.D. in toxicology or a related biological science, such as physiology, pharmacology, etc. Furthermore, the candidate is expected to have a minimum of 5 years of relevant experience in a high-performance pharmaceutical/biotechnology environment. Experience in advancing both oncology and non-oncology projects, in the U.S. and Europe, is highly desirable but not a requirement. DABT certification is desirable but not a requisite. The role demands a highly goal-driven approach and the ability to focus on time-sensitive objectives. The candidate should also enjoy operating in an exceptionally dynamic and cooperative environment.
Please quote job reference: PD-001 when responding to this advertisement.
Qualified candidates should apply with a CV and cover letter
