Preclinical Operations Specialist (GLP, Pharma/Biotech, REMOTE) (v010)

  • Contract Duration: 6+ months, REMOTE
  • Research & Development
  • Boston, MA

Website Lenox Executive Search


6+ month REMOTE Contract role with potential to extend. EST working hours required. 2-5 years experience in Pharma/Biotech industry.

Lenox Executive Search is seeking an experienced Preclinial Operaions Specialist to fill an 6+ month contractual role with a global pharmaceutical company. Seeking candidates who have GLP (Good Laboratory Practices) experience.

REQUIREMENTS of the Preclinical Operations Specialist:

  • Bachelor’s degree in relevant discipline
  • 2-5 years’ experience relevant experience
  • Pharma/biotech experience REQUIRED
  • Seeking candidates with knowledge of GLP (Good Laboratory Practices)
  • Preferably CRO experience
  • Detail oriented, deadline driven
  • Ability to work independently
  • Experience with Smartsheet preferred
  • Bonus to have Microsoft Project
  • Effective communicator (written and verbal) to exchange straightforward information within a defined area
  • Ability to multitask effectively to manage efforts on multiple projects

RESPONSIBILITIES of the Preclinical Operation Specialist:

The Preclinical Operations Specialist performs a variety of well-defined support functions for management of nonclinical studies, or aspects thereof, within Research, Pharmaceutical, and Preclinical Sciences (RPPS). Working in concert with a program representative, the incumbent will perform program management activities, with supervisor oversight, in support of the Company’s research and development goals.

  • Under direction of supervisor, participates in limited areas of development projects and/or timelines, which vary in function and scope
  • May be responsible for limited independent initiatives, working with supervisor in setting the objectives of these initiatives
  • May perform administrative functions (scheduling internal and external meetings)
  • Troubleshoots routine problems
  • Provides management of aspects of outsourced, or insourced, projects including scheduling timelines
  • Performs quality control of routine documents
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