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Job Summary: The candidate will design and perform experiments in order to develop chemical processes for the manufacture drug substances. You will be expected to subsequently undertake the GMP manufacture of these API processes at kilo-lab scale and support manufacture at a CMO7/30/2015 Lexington, MA Save This Job
Job Summary: The Clinical Scientist as a member of the clinical team will support development strategies for drug candidates and help execute clinical trials. This position reports to the VP, Clinical Development. Responsibilities: ? Works closely with VP, Clinical Development,7/30/2015 Lexington, MA Save This Job
Job Summary: The position will provide support for the Quality Assurance group. The candidate will work with cross functional teams to maintain internal quality systems with an emphasis on GCP. Responsibilities: ? Perform routine QA review of Clinical Protocols, Clinical Study7/30/2015 Lexington, MA Save This Job
Job Summary: The Scientist/Senior Scientist position will be responsible for leading and/or performing all analytical chemistry development tasks within one or more small-molecule CMC development programs, including method development and validation, analytical investigations,6/30/2015 Lexington, MA Save This Job
Job Summary: Works closely with Vice President, Product Planning & Program Management on the oversight and management of clinical-stage drug development programs. Responsibilities: ? Create and maintain integrated project plans for Phase 2 and Phase 1 clinical drug development6/30/2015 Lexington, MA Save This Job