Toxicology Expert

About Merrimack PharmaceuticalsMerrimack Pharmaceuticals is a high-energy biotechnology company focused on the discovery and development of transformational medicines for complex disease. Our work is founded on revolutionary drug discovery platform that integrates high throughput quantitative proteomics, computational biology, and chemical engineering into a singular capability to dissect complex biological systems with unparalleled productivity. We are now seeking talented and motivated individuals to join us in our efforts to develop new medicines for cancer and diseases of the immune system. Oversee pre-clinical activities to support Oncology and MM-093 programs. Specific responsibilities include: Design pre-clinical development strategies and studies to support the initiation of Phase 1 trials of new anticancer agents (MM-121, MM-111, etc.) and ongoing development of MM-093 in multiple indications Identify and manage CRO’s, including negotiating budgets Oversee final data analysis and report writing for all pre-clinical activities Contribute to the preparation of regulatory documents including IB’s, IND’s and annual reports

The ideal candidate will a Ph.D. degree in Pharmacology, Toxicology, Biochemistry, or equivalent (M.D, D.V.M.) with 3 – 5 years post-doctoral training and industrial experience in pharmacology or toxicology. Prior experience with biologics and IND preparation is necessary; BLA, NDA and/or MAA experience is preferred. You will have excellent communication and organization skills demonstrated by your experience in analysis and interpretation of experiments for the evaluation of pre-clinical candidates as well as having managed outside vendors. Especially desired are enthusiastic, flexible people who like the challenge of working with a variety of teams in a multi-disciplinary environment. Equally important are strong interpersonal skills and an entrepreneurial spirit.