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ÕÐÆ¸in vivo pharmacology director - Diabetes
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Duties and Responsibilities • Working with IVP and local site leadership to develop site IVP service strategy and execute the plan. • Accountable for development and growth of the site IVP services. • Engage with new and existing clients in collaboration with account executives to develop solutions to client study needs • Train technical staff in the conduct of in vivo models and methods • Develop study protocols and ensure that the protocol, including any changes, is approved and complies with appropriate SOPs, GRP/GLPs, and regulatory agency guidelines • Develop study protocols aligned with IACUC requirements to support internal and external projects. • Coordinate efforts of study teams in the execution of client studies • Monitor progress and status of studies. Ensure that all experimental data and relevant events, including unanticipated findings, errors and deviations, are accurately recorded and are reconstructable • Preparation of study reports, including incorporation and review of contributor reports, for review and submission to clients • Participate in or hosts client visits • Support internal and/or client QA audits Education/Qualifications • PhD in Pharmacology or relevant and equivalent degree. Experience • 5-8or more years of relevant drug discovery experience in a pharmaceutical or biotechnology company setting • In vivo model expertise and experience required • Experience in Diabetes and Metabolic Disease research and models preferred • Experience in leading and coordinating study conduct in a matrixed resource environment preferred |
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