THE LARGEST COLLECTION OF JOBS ON EARTH
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Associate Director, Nonclinical Pharmacokinetics & Bioanalytical Analysisn nIn this position you will be responsible for developing and validating bioanalytical methods to support GXP pharmacokinetic and pharmacodynamic assessments for large molecule..
Sr. Director, Regulatory Affairs CMC n n nThis position is responsible for the CMC strategic regulatory direction, interactions with U.S. and international regulatory agencies, regulatory CMC submissions, and operational CMC..
Scientist II, Formulations Developmentn nGood things are happening at Omeros!n nCome join our CMC Team!n n nThis position will be responsible for formulation development of monoclonal antibodies to support preclinical,..
Scientist I, Analytical Developmentn n nThe Scientist I, Analytical Development will primarily be responsible for the development, transfer, qualification, and validation of potency bioassays in support of clinical development and..
nScientist I, Analytical Developmentn nThis position will primarily be responsible for the development, transfer, qualification, and validation of potency bioassays in support of clinical development and commercialization of antibody therapeutics...
Toxicology Study MonitornReporting to the Sr. Director, Toxicology in our Non-Clinical Group, you will be responsible for the management and oversight of contract research organization (CRO) work including contributions to..
Senior Director, Regulatory Affairs n nThis position is responsible for overseeing, supervising, and managing the Regulatory Affairs (RA) function. This includes Regulatory CMC, Regulatory Program Management, Regulatory Submissions, Regulatory Information,..