Responsibilities

• The successful candidate will manage global and EU focused project activities required to license Zoetis products or to achieve project team milestones. In that capacity, he/she will be responsible for the overall conduct of clinical studies in support of Zoetis R&D project(s) with focus on pharmaceutical and bio-pharmaceutical products. The activities include but are not limited to budgeting, site selection, animal sourcing, resource planning, timeline management, request of legal documentation, protocol and report development, supply planning, and study monitoring.• The successful candidate will manage multiple studies and/or projects. In these capacities, the successful candidate will facilitate (sub)team meetings, represent the (sub)team to the larger project team or to R&D management.• The successful candidate is expected to independently assess challenges and prepare complex decisions with innovative solutions.• In the role, the successful candidate will provide training to internal and external collaborators.• The successful candidate is expected to prepare manuscripts for publication in international scientific journals, presentations for external meetings and documents supporting regulatory submissions globally.• The successful candidate will participate in and/or lead multi-functional teams within and across disciplines that include representation from Manufacturing, Regulatory Affairs, Formulation, Safety Sciences and Analytics, and Marketing.• The successful candidate will work with R&D leadership team(s) to implement best practices leading to increased efficiencies .Education and experience Qualification (Essential)• Degree in Veterinary Medicine• Understanding of scientific research principles and interpretation of research results, preferably demonstrated by PhD or equivalent Experience (Desirable)• Work experience with Good Clinical Practice for Veterinary Trials (GCPv) and/or Good Laboratory Practice (GLP)• Active participation in scientific (preferably veterinary) research projects• An understanding of veterinary drug development Technical and Interpersonal skills requirements Technical abilities (Essential)• Fluent in English (spoken and written). Knowledge of any other language is considered as a plus.• Attention to detail.• Strong ability to organize, plan and prioritize effectively.• Ability to work on different concurrent studies and projects.• Ability to give day-to-day directions to study participants and team members.• Excellent presentation and writing skills. Interpersonal skills (Essential)• Strong team player.• Professional and mature listening and communication skills.• Interpersonal and multi-cultural savvy, as demonstrated by the ability to work effectively with colleagues from a diverse background.• Strong awareness around Diversity, Equity and Inclusion.• Ability to generate and drive a team driven result. Physical Position Requirements• Fully qualified driver in order to visit study sites.• Ability to travel regularly (up to 20%) and independently nationally and internationally (mainly EU).• Willingness to work flexible hours