Pharmacology Study Director

3 weeks ago


Worcester, Massachusetts, United States Charles River Laboratories Full time

We are seeking a skilled and passionate Pharmacology Study Director to provide scientific leadership for all technical aspects of studies.

The qualified candidate will work closely with our clients and our established teams in the design, conduct, analysis, interpretation, and reporting of a wide variety of Oncology studies in a fast-paced and dynamic environment.

Responsibilities of this position include extensive interaction and communication with client scientists in the discovery oncology research area of study management, interpretation, and reporting.

Key Responsibilities:

  • Expertise in in-vivo animal skills necessary to support xenograft oncology studies.
  • Ability to set-up and validate in vivo cancer models (xenograft rodent models).
  • Evaluate anticancer NCEs for pharmacokinetic/pharmacodynamics/efficacy in xenograft models.
  • Conduct and oversee in vivo studies for efficacy and target inhibition (tumor implantation/inoculation, compound dosing, tumor excision/biopsy).
  • Generate high-quality protocols, amendments, and reports appropriate for assigned studies.
  • Review, interpret, integrate, and present data on assigned studies, using the assistance of senior scientific staff as appropriate.

Requirements:

  • Possess strong interpersonal skills with strong scientific curiosity, initiative, and resourcefulness.
  • Possess exceptional organizational and planning skills enabling management of multiple, concurrent tasks and priorities.
  • Be team-oriented, highly collaborative, and have a results-oriented focus.
  • Be self-driven and enthusiastic with the ability to thrive in a dynamic environment.

Education and Experience:

  • Bachelor's degree (B.S./B.A.) or equivalent in a scientific related discipline.
  • Related Master's degree (M.S./M.A.) or PhD/DVM preferred.
  • Minimum of 6 years related experience in the contract research, academic, or pharmaceutical industry required.

Additional Requirements:

  • Understanding of regulatory requirements of study types assigned, as well as Testing Facility BOPs and the Good Laboratory Practices (GLPs), as appropriate.
  • Demonstrate leadership skills as they pertain to intra- and interdepartmental initiatives, Sponsor interactions, and business development.
  • Effective written and verbal communication skills.
  • Ability to handle multiple projects, prioritize work, and meet deadlines.
  • Proficiency in the use of standard software including Microsoft Excel, Word, PowerPoint, etc., and with standard laboratory calculations.


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