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Clinical Development Cambridge, MA, United States Merrimack is a fully integrated biopharmaceutical company that views cancer as a complex engineering challenge. Through systems biology, which brings together the fields of biology, computing and engineering, Merrimack aims to3/14/2016 Cambridge, MA Save This Job
Scope of Responsibilities The role of the Global Safety Lead (GSL) is establishing the strategy, direction and pharmacovigilance activities for assigned products. Specific Duties Provides global medical leadership and input into all aspects of safety of assigned product(s)3/31/2016 San Francisco, CA Save This Job
Company Overview Relypsa, Inc. is a biopharmaceutical company focused on the discovery, development and commercialization of polymeric medicines for patients with conditions that are often overlooked and undertreated and can be addressed in the gastrointestinal tract. The4/8/2016 Redwood City, CA Save This Job
Scope of Responsibilities The role of the Medical Case Reviewer within Drug Safety is to perform individual case assessment and evaluation of serious adverse events (SAEs) and special reporting situations, and to ensure that appropriate safety information is captured in the3/31/2016 San Francisco, CA Save This Job
Req Id 3421 - Posted 03/25/2016 - United States - Massachusetts - Cambridge - Regulatory Affairs The Director, Regulatory Affairs, REMS, is responsible for providing strategic and operational leadership for the Risk Evaluation and Mitigation Strategies (REMS) for the Company?s4/14/2016 Cambridge, MA Save This Job
Reporting to the Chief Medical Officer, the Senior Clinical Trial Manager will be responsible for the day-to-day management of ChemoCentryx clinical trials, including management of contract CROs conducting company sponsored clinical trials. Specific Responsibilities Work with3/28/2016 Mountain View, CA Save This Job