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Research Associate

Boston Metro Area, MA

Post Date: 02/16/2017 Job ID: JN -022017-18398
  • Responsible for the design, execution, interpretation, and reporting of preclinical pharmacology and pharmacokinetic studies to the standard required for regulatory documents and filings.
  • Responsible for oversight during the pre-study process (drafting a protocol/study design, preparing documents for data collection, and conducting a pre-initiation meeting), study execution, data analysis, interpretation, and reporting (including data presentations and authoring study reports).
  • In addition, given the nature of these studies and the potential for inclusion in regulatory filings, the Associate will also interact closely with Regulatory and Quality colleagues.
Experience: 6+ years

  • Animal handling and relevant laboratory experience required, including rodent handling, dosing and blood sampling techniques, and test article formulation.
  • Strong time management skills, ability to multi-task, excellent verbal and written communication skills, and an established ability to collaborate effectively in a multidisciplinary environment.
  • Previous experience in drug development.
Education: B.S. in a biological science

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