Pharmacology Study Director
4 weeks ago
About the Role
We are seeking a skilled and passionate Pharmacology Study Director to provide scientific leadership for all technical aspects of studies. This role will involve working 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
- 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
- Bachelor's degree (B.S./B.A.) or equivalent in a scientific related discipline.
- Minimum of 6 years related experience in the contract research, academic or pharmaceutical industry.
- Strong interpersonal skills with strong scientific curiosity, initiative, and resourcefulness.
- Exceptional organizational and planning skills enabling management of multiple, concurrent tasks & priorities.
- Team orientated, highly collaborative, and results-oriented focus.
- Self-driven and enthusiastic with the ability to thrive in a dynamic environment.
About Charles River
Charles River Laboratories is an early-stage contract research organization (CRO) with a diverse portfolio of discovery and safety assessment services. We have built upon our foundation of laboratory animal medicine and science to develop a comprehensive, integrated portfolio that employs the latest technology and platforms to provide chemistry, biology, and pharmacology services that support clients from the earliest stages of hit identification all the way through to IND.
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