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Company: Job Juncture
Location: Rockville
Posted on: June 15, 2022

Job Description:

My biotech client is expanding and seeks a preclinical scientist to take on the following tasks:

  • Serve on project teams focused on developing novel therapeutic drugs and targets.
  • Act as the scientific and technical reviewer for nonclinical studies performed with external collaborators or CROs.
  • Write and edit nonclinical study protocols.
  • Oversee review of nonclinical study reports and finalize study reports to ensure appropriate interpretation and reporting of data.
  • Build and develop partnerships with CROs.
  • Write and review nonclinical safety documentation, including IBs, INDs and BLAs.
  • Communicate with regulatory agencies to resolve nonclinical issues.

    The ideal candidate will possess the following qualities:

    • MS/PhD and 2+ years of toxicological related sciences in academia or industry setting.
    • Experience in organizing, analyzing, and documenting nonclinical studies.
    • Ability to organize and analyze multidisciplinary data sets.
    • Available to travel to CROs for study monitoring activities.
    • Working knowledge of regulatory guidelines relevant to preclinical development.
    • Understanding of FDA and GLP.

Keywords: Job Juncture, Rockville , Toxicologist, Other , Rockville, Maryland

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