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Job Summary: Works closely with VP, Clinical Operations for the oversight and execution of assigned clinical studies Responsibilities: Contribute in the development/writing of Clinical Protocol Contribute in the review of all study related documentation (Clinical Protocol,7/7/2014 Lexington, MA Save This Job
Job Summary: The Associate Director should possess a strong in vitro and in vivo pharmacology background combined with significant drug development experience. The Associate Director will have the opportunity to work across multiple therapeutic areas including CNS, fibrosis,7/7/2014 Lexington, MA Save This Job
Description: This is an experienced-level position within the CMC Group at Concert. The Senior Scientist I/II will be responsible for formulation development activities within one or more small-molecule CMC development programs, including pre-formulation experiments,7/7/2014 Lexington, MA Save This Job
Description: The Director / Associate Director, Analytical Chemistry is responsible for all analytical chemistry within the CMC Group, including method development, validation, analytical investigations and process and product characterization. For this role s/he will have7/7/2014 Lexington, MA Save This Job
Description: The Senior Biostatistician will be working within cross?functional program teams as the statistical lead, responsible for statistical activities across multiple studies reporting to the Program Director. The ideal candidate is high-energy, self-motivated,7/7/2014 Lexington, MA Save This Job
Job Summary: Works closely with Senior Director, 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 development programs, including7/7/2014 Lexington, MA Save This Job