This role supports Millipore Sigma’s BioReliance Genetic Toxicology services.
The Study Director will perform all aspects of the GLP role of Study Director with overall scientific responsibility for the study design, interpretation and reporting study results. The role will also serve as a scientific resource in Genetic Toxicology and is responsible for the study design interpretation and reporting of study results. You will interact with sponsors or clients to present and interpret results, and to ensure the client expectations are met or exceeded. You will also provide technical advice and support for internal and external interactions such as client and regulatory audits/inspections, meetings, teleconferences. You will also contribute to and author scientific publications and presentations at conferences/ seminars. This role will also monitor industry trends to ensure that Millipore Sigma remains at the forefront in the field of Genetic Toxicology and review and recommend potential assay developments to upper management. You will lead by example, offer scientific insight to other staff members, and promote a culture of continuous improvement. You will participate in initiatives and/or projects to drive improvement in quality and/or client service.
Who you are:
MA/MS in scientific discipline with 6+ years of industry experience within genetic toxicology.
Relevant working knowledge and experience in executing and overseeing technical projects.
Laboratory Experience in conducting and/or overseeing GLP-regulated studies.
External customer facing experience.
Ph.D. in scientific discipline with 2+ of industry experience in genetic toxicology.
In vivo micronucleus, Ames assay, chromosomal aberration experience.
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