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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,10/23/2016 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,10/23/2016 Lexington, MA Save This Job
Job Description: Works closely with the Clinical Development team for the oversight and execution of assigned clinical studies ?May be responsible for one or more concurrent clinical studies ?Contribute in the development of the clinical study design and writing of the study10/23/2016 Lexington, MA Save This Job
Job Summary: Working within the clinical development organization, the Scientist will support multiple programs, performing PK analyses for Phase 1 studies and provide input to the development of clinical study designs and protocols. A strong background in pharmacokinetics10/23/2016 Lexington, MA Save This Job
Job Summary: Performs the coordination and preparation of document packages for regulatory submissions for new and mature products to ensure alignment and compliance with local and regional registration requirements as well as with company policies from all areas of company as10/23/2016 Lexington, MA Save This Job
Job Summary: This is a laboratory-focused, experienced position within the Formulation Development Group at Concert Pharmaceuticals in Lexington, MA. The Scientist/Senior Scientist will be responsible for formulation development activities within one or more small-molecule10/23/2016 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 for GxP activities. Responsibilities: ? Write, review and approve Standard Operating Procedures (SOP) and Forms10/23/2016 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 development10/23/2016 Lexington, MA Save This Job