), Clinical Research Associates (CRAs), and Clinical Trial Associates (CTCs). Responsibilities include managing site and vendor matters in collaboration with Clinical Program Managers, under the supervision of the Assoc

IDEAL PROFILE: Education: University degree or equivalent (Medical, MBA, or Marketing preferred, but not essential). Experience: Proven track record in clinical research, with deep understanding of international clinical trial

Qualifications (education, experience and/or training, required certifications): • DVM and PhD, or Master and PhD in a relevant field or equivalent • 5+ years of R&D experience, including clinical trial management and/or

Qualifications (education, experience and/or training, required certifications): • DVM and PhD, or Master and PhD in a relevant field or equivalent • 5+ years of R&D experience, including clinical trial management and/or